View Products
| IBI Reagents | |
|
|
| IBI Reagents - Acrylamide Gel Catalysts and Oxidizers | |
|
|
|
|
|
|
|
Ammonium Persulfate is a potent oxidizer that promotes polymerization of acrylamide gels by scavenging dissolved oxygen in the gel solution, thereby accelerating the acrylamide/bisacrylamide reaction. Click on details to view Specification |
|
|
|
|
|
TEMED is used as a catalyst for polymerization of polyacrylamide gels. Click on details to view Specification |
|
| IBI Reagents - Acrylamide Powders | |
| IBI offers high purity acrylamide powder in several convenient sizes. From 100gm to 3Kg IBI has the acrylamide you lab is looking for! |
|
|
|
|
|
Acrylamide is the primary component of polyacrylamide gels. IBI offers highly purified acrylamide powders to offer today's researcher the flexibility of mixing any concentration or ratio desired. Click on details to view Specification |
|
|
|
|
|
Acrylamide is the primary component of polyacrylamide gels. IBI offers highly purified acrylamide powders to offer today's researcher the flexibility of mixing any concentration or ratio desired. Click on details to view Specification |
|
|
|
|
|
Acrylamide is the primary component of polyacrylamide gels. IBI offers highly purified acrylamide powders to offer today's researcher the flexibility of mixing any concentration or ratio desired. Click on details to view Specification |
|
|
|
|
|
Acrylamide is the primary component of polyacrylamide gels. IBI offers highly purified acrylamide powders to offer today's researcher the flexibility of mixing any concentration or ratio desired. Click on details to view Specification |
|
| IBI Reagents - Acrylamide:Bisacrylamide Powders | |
| IBI offers premixed acrylamide:bisacrylamide powders in 19:1, 29:1, and 37.5:1 ratios. Just add ddi water to these premixed powders for the % solution you desire. |
|
|
|
|
|
Acrylamide:Bisacrylamide 19:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 19:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
|
|
|
|
Acrylamide:Bisacrylamide 19:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 19:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
|
|
|
|
Acrylamide:Bisacrylamide 29:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 29:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
|
|
|
|
Acrylamide:Bisacrylamide 29:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 29:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
|
|
|
|
Acrylamide:Bisacrylamide 37.5:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 37.5:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
|
|
|
|
Acrylamide:Bisacrylamide 37.5:1 powder is the primary component of polyacrylamide gels. The powder is premixed to a 37.5:1 ratio, and by adding ddi water directly into the bottle you will have created a 30% or 40% solution that is ready to use. See Specification Sheet for amounts of ddi water to add for proper mixtures. Click on details to view Specification |
|
| IBI Reagents - Bisacrylamides | |
|
|
|
|
|
|
|
Bisacrylamide is used in polyacrylamide gels for sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
Bisacrylamide is used in polyacrylamide gels for sequencing and protein electrophoresis. Click on details to view Specification |
|
| IBI Reagents - INSTAPAGE Liquid Acrylamide Solutions | |
| IBI offers a full line of 30 and 40% INSTAPAGE liquid acrylamide solutions. INSTAPAGE solutions are available in convenient 19:1, 29:1, and 37.5:1 ratios as well to suit many different applications. |
|
|
|
|
|
InstaPAGE-30% (19:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-30% (19:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-30% (29:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-30% (29:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-30% (37.5:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-30% (37.5:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (19:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (19:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (29:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (29:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (37.5:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
InstaPAGE-40% (37.5:1) acrylamide solution is a premixed acrylamide:bisacrylamide solution for pouring polyacrylamide gels used in sequencing and protein electrophoresis. Click on details to view Specification |
|
|
|
|
|
Acryliquid-40 and InstaBIS-2 can be used to make 19:1, 29:1, and 37.5:1 acrylamide/bisacrylamide solutions. Click on details to view Specification |
|
|
|
|
|
Acryliquid-40 and InstaBIS-2 can be used to make 19:1, 29:1, and 37.5:1 acrylamide/bisacrylamide solutions. Click on details to view Specification |
|
| IBI Reagents - IBI Agarose | |
|
IBI agarose is produced to deliver lot-to-lot consistency, quality and purity. Packaged in numerous sizes from 25g to 1kg. IBI is sure to have the package size you require at the best price! If you're looking to purchase multiple units please feel free to phone us for special pricing opportunities! |
|
|
|
|
|
|
|
|
|
|
|
IBI Molecular Biology Grade Agarose is highly refined and highly purified. Each lot is physically tested and verified for performance in its designated application. IBI applies strict testing parameters to insure lot to lot consistancy. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Agarose is highly refined and highly purified. Each lot is physically tested and verified for performance in its designated application. IBI applies strict testing parameters to insure lot to lot consistancy. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Agarose is highly refined and highly purified. Each lot is physically tested and verified for performance in its designated application. IBI applies strict testing parameters to insure lot to lot consistancy. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Agarose is highly refined and highly purified. Each lot is physically tested and verified for performance in its designated application. IBI applies strict testing parameters to insure lot to lot consistancy. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Agarose is highly refined and highly purified. Each lot is physically tested and verified for performance in its designated application. IBI applies strict testing parameters to insure lot to lot consistancy. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI Molecular Biology Grade Low Melt Agarose is commonly used as a gel matrix when fragment recovery after electrophoresis is desired. It can also be used for preparing large DNA samples for plugs. Click on details to view Specification |
|
|
|
|
|
IBI 3:1 Super Sieve is designed for analytical electrophoresis where high resolution is needed DNA 100 - 1500bp and PCR products <1000bp can be resolved. IBI Super Sieve agarose has a low viscosity so high concentration gels can be made with high resolving capacity. |
|
|
|
|
|
IBI 3:1 Super Sieve is designed for analytical electrophoresis where high resolution is needed DNA 100 - 1500bp and PCR products <1000bp can be resolved. IBI Super Sieve agarose has a low viscosity so high concentration gels can be made with high resolving capacity. IB70053 = 250g size |
|
|
|
|
|
IBI Ultra Sieve agarose is designed for high resolution electrophoresis where resolutions of polyacrylamide gel is needed. Ultra Sieve agarose improves clarity of gels and enhances visualization, even at high concentrations. For best reults, Ultra Sieve gels should be chilled at 4 - 8 deg C for 30 minutes before use. Ideal for seperations between 10 - 1200 bp at concentrations between 1.8% and 5% in 1X TAE To improve resolution capacity for smaller sizes TBE buffer should be used. |
|
|
|
|
|
IBI Ultra Sieve agarose is designed for high resolution electrophoresis where resolutions of polyacrylamide gel is needed. Ultra Sieve agarose improves clarity of gels and enhances visualization, even at high concentrations. For best reults, Ultra Sieve gels should be chilled at 4 - 8 deg C for 30 minutes before use Ideal for seperations between 10 - 1200 bp at concentrations between 1.8% and 5% in 1X TAE To improve resolution capacity for smaller sizes TBE buffer should be used. |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
|
|
|
|
IBI's PFGE Agarose is a linear polymer with a very high molecular weight, thus giving gel structures unlike those of traditional agaroses. This characteristic, added to the very low sulfate content, produces a strong intercatenary interaction, yielding a gel with a very high gel strength and higher exclusion limit. Click on details to view Specification |
|
| IBI Reagents - IBI Alcohols | |
|
IBI Alcohols are known for their lot-to-lot consistency and purity. Packaged in several different sizes to fit the needs of small to large users. Quality, convenience and priced to stretch your research Dollars. Call us for multi-unit purchase discounts! |
|
|
|
|
|
Ethanol is widely used for precipitating nucleic acids. The nucleic acid precipitate, which is formed in the presence of moderate concentrations of monovalent cations, is recovered by centrifigution and redissolved in an appropriate buffer at the desired concentration. Denatured with 5% methanol. Click on details to view Specification |
|
|
|
|
|
Ethanol is widely used for precipitating nucleic acids. The nucleic acid precipitate, which is formed in the presence of moderate concentrations of monovalent cations, is recovered by centrifigution and redissolved in an appropriate buffer at the desired concentration. Denatured with 5% methanol. Click on details to view Specification |
|
|
|
|
|
Ethanol is widely used for precipitating nucleic acids. The nucleic acid precipitate, which is formed in the presence of moderate concentrations of monovalent cations, is recovered by centrifigution and redissolved in an appropriate buffer at the desired concentration. Denatured with 5% methanol. Click on details to view Specification |
|
|
|
|
|
Isopropanol is widely used for precipitating nucleic acids. The nucleic acid precipitate; which is formed in the presence of moderate concentrations of monovalent actions, is recovered by centrifugation and redissolved in an appropriate buffer at the desired concentrations. Click on details to view Specification |
|
|
|
|
|
Isopropanol is widely used for precipitating nucleic acids. The nucleic acid precipitate; which is formed in the presence of moderate concentrations of monovalent actions, is recovered by centrifugation and redissolved in an appropriate buffer at the desired concentrations. Click on details to view Specification |
|
|
|
|
|
Methanol is commonly used for Western Blotting Applications. Click on details to view Specification |
|
|
|
|
|
Methanol is commonly used for Western Blotting Applications. Click on details to view Specification |
|
|
|
|
|
Methanol is commonly used for Western Blotting Applications. Click on details to view Specification |
|
|
|
|
|
Methanol is a high purity, functionally tested reagent suitable for HPLC work. It has low UV absorption and low particulate count to reduce background. Click on details to view Specification |
|
|
|
|
|
Isobutanol is used to extract ethidium bromide from nucleic acid solutions and to concentrate , DNA in aqueous solutions. It is also used to overlay polyacrylamide gels to prevent oxidation. Click on details to view Specification |
|
| IBI Reagents - IBI Antibiotics | |
|
|
|
|
|
|
|
Ampicillin inhibits cell wall biosynthesis (peptidoglycan cross-linking). Stock solution of antibiotics dissolved in water should be sterilized by filtration through a 0.22 micron filter. Click on details to view Specification |
|
|
|
|
|
Carbenicillin is an antibiotic which inhibits bacterial cell wall synthesis, activity against gram-positive and gram-negative bacteria, and for cell culture media applications. Recommended use is 100mg/ml. Stock solution of antibiotics dissolved in water should be sterilized by filtration through a 0.22 micron filter. Click on details to view Specification |
|
|
|
|
|
Carbenicillin is an antibiotic which inhibits bacterial cell wall synthesis, activity against gram-positive and gram-negative bacteria, and for cell culture media applications. Recommended use is 100mg/ml. Stock solution of antibiotics dissolved in water should be sterilized by filtration through a 0.22 micron filter. Click on details to view Specification |
|
|
|
|
|
Chloramphenicol is used in the amplification of plasmids and colony hybridizations. Antibiotics dissolved in ethanol need not be sterilized. Click on details to view Specification |
|
|
|
|
|
Gentamycin Sulfate Solution is used as an inhibitor for the growth of a wide variety of gram-positive and gram-negative microorganisms. It is intended for research only. The bottle concentration is 50mg/ml. Click on details to view Specification |
|
|
|
|
|
Kanamycin Sulfate is used to bind to 70S ribosomal subunit, inhibits translocation, and elicits miscoding bactericidal. Kanamycin Sulfate is derived via microbial fermentation. No animal products or by-products are used in the manufacturing process or fermentation media. Stock solution of antibiotics dissolved in water should be sterilized by filtration through a 0.22 micron filter. Click on details to view Specification |
|
|
|
|
|
Streptomycin Sulfate is used to bind to S12 protein and 30S ribosomal subunit, inhibits translocation, and elicits miscoding batericidal. Stock solution of antibiotics dissolved in water should be sterilized by filtration through a 0.22 micron filter. Click on details to view Specification |
|
|
|
|
|
Tetracycline Hydrochloride inhibits protein synthesis (elongation) by preventing the binding of aminoacyl-tRNA to ribosome. Bacteriostatic. Antibiotics dissolved in ethanol need not be sterilized. Magnesium ions are antagonists of tetracycline. Use media without magnesium salts (e.g. LB medium) for the selection of bacteria resistant to tetracycline. Click on details to view Specification |
|
| IBI Reagents - IBI Buffer Components | |
|
|
|
|
|
|
|
Tris is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Tris is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Tris is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Tris-HCl is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Glycine is a neutral amino acid. It is the primary component in polyacrylamide buffers. During the process of separation the glycine forms an electrical front which pulls the marcomolecules along. Click on details to view Specification |
|
|
|
|
|
EDTA is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Tris-HCl is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
EDTA Solution is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
EDTA Solution is commonly used in biological and electrophoresis buffer systems. Click on details to view Specification |
|
|
|
|
|
Boric Acid is an ingredient in Tris-Borate buffer systems, used in high voltage electrophoresis. Click on details to view Specification |
|
|
|
|
|
Ammonium Acetate is a salt commonly used in the precipitation of nucleic acids. Click on details to view Specification |
|
|
|
|
|
Urea is used as a nucleic acid and protein denaturant in polyacrylamide gel electrophoresis. It has a standard concentration of 6 to 8M. Click on details to view Specification |
|
|
|
|
|
Urea is used as a nucleic acid and protein denaturant in polyacrylamide gel electrophoresis. It has a standard concentration of 6 to 8M. Click on details to view Specification |
|
|
|
|
|
DTT is used in enzyme preparations to prevent formation of disulfides from sulfhydryl group, thereby stabilizing the enzyme. Click on details to view Specification |
|
|
|
|
|
DTT is used in enzyme preparations to prevent formation of disulfides from sulfhydryl group, thereby stabilizing the enzyme. Click on details to view Specification |
|
|
|
|
|
HEPES, Sodium Salt is a zwintterionic buffer ideally suited for cell culture in a range of 10 to 25mM. HEPES has a buffering range from 6.8 to 8.2. Click on details to view Specification |
|
|
|
|
|
HEPES, Free Acid is a zwitterionic buffer ideally suited for cell culture in a range of 10 to 25mM. HEPES also has a buffering range of 6.8 to 8.2. HEPES is also a key component of Tris-HEPES buffer, used during electrophoresis of polyacrylamide gels. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
HEPES, Free Acid is a zwitterionic buffer ideally suited for cell culture in a range of 10 to 25mM. HEPES also has a buffering range of 6.8 to 8.2. HEPES is also a key component of Tris-HEPES buffer, used during electrophoresis of polyacrylamide gels. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
HEPES, Free Acid is a zwitterionic buffer ideally suited for cell culture in a range of 10 to 25mM. HEPES also has a buffering range of 6.8 to 8.2. HEPES is also a key component of Tris-HEPES buffer, used during electrophoresis of polyacrylamide gels. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
HEPES, Free Acid is a zwitterionic buffer ideally suited for cell culture in a range of 10 to 25mM. HEPES also has a buffering range of 6.8 to 8.2. HEPES is also a key component of Tris-HEPES buffer, used during electrophoresis of polyacrylamide gels. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
Sucrose is used in rate-zonal centrifugation to separate molecules, based on size and conformation. Click on details to view Specification |
|
|
|
|
|
MOPS is a zwitterionic buffer ideally suited for RNA electrophoresis in agarose gels. Having a buffering range 6.5 - 7.9, MOPS works exceptionally well in formaldehyde gels at a concentration of 20nM. DEPC is added to ensure the buffer is nuclease contamination free. Use sterile water to dilute 10X solution, if required. Click on details to view Specification |
|
|
|
|
|
MOPS is a zwitterionic buffer ideally suited for RNA electrophoresis in agarose gels. Having a buffering range 6.5 - 7.9, MOPS works exceptionally well in formaldehyde gels at a concentration of 20nM. DEPC is added to ensure the buffer is nuclease contamination free. Use sterile water to dilute 10X solution, if required. Click on details to view Specification |
|
| IBI Reagents - IBI PreMixed Buffers | |
|
|
|
|
|
|
|
TBE Buffer's significantly greater buffering capacity (relative to TAE) eliminates the need for recirculation in all but the most extended runs. This attribute makes TBE the buffer of choice for DNA sequencing and other extended electrophoresis applications. Click on details to view Specification |
|
|
|
|
|
TBE Buffer's significantly greater buffering capacity (relative to TAE) eliminates the need for recirculation in all but the most extended runs. This attribute makes TBE the buffer of choice for DNA sequencing and other extended electrophoresis applications. Click on details to view Specification |
|
|
|
|
|
TBE Buffer's significantly greater buffering capacity (relative to TAE) eliminates the need for recirculation in all but the most extended runs. This attribute makes TBE the buffer of choice for DNA sequencing and other extended electrophoresis applications. Click on details to view Specification |
|
|
|
|
|
TBE's significantly greater buffering capacity (relative to TAE) eliminates the need for recirculation in all but the most extended runs. This attribute makes TBE the buffer of choice for DNA sequencing and other extended electrophoresis applications. Click on details to view Specification |
|
|
|
|
|
The 10X TBE Buffer Pouch makes 1L of 10X TBE Buffer Solution. Add ddi water until a pH level of 8.1 to 8.5 has been reached. TBE Buffer has a significantly greater buffering capacity (relative to TAE) that eliminates the need for recirculation in all but the most extended electrophoresis runs. Click on details to view Specification |
|
|
|
|
|
TAE Buffer is commonly used in low voltage DNA electrophoresis applications. It's relatively low buffering capacity will become exhausted in extended or high current runs, making buffer recirculation necessary in such runs. Click on details to view Specification |
|
|
|
|
|
25X TAE Buffer is commonly used in low voltage electrophoresis runs. By adding 1L of ddi water to this buffer pouch, you will produce approximately 1L of 25X TAE Buffer Solution. Click on details to view Specification |
|
|
|
|
|
10X Tris-Glycine Buffer is used for polyacrylamide electrophoresis. It can be used in both native and denaturing (SDS) polyacrylamide gel electrophoresis of proteins. The versatility of Tris-Glycine Buffer enables the accurate separation of proteins in the range of 5 - 500kDa. Click on details to view Specification |
|
|
|
|
|
10X Tris-Glycine-SDS Buffer is used for polyacrylamide electrophoresis. It can be used in both native and denaturing (SDS) polyacrylamide gel electrophoresis of proteins. The versatility of Tris-Glycine Buffer enables the accurate separation of proteins in the range of 5-500kDa. Click on details to view Specification |
|
|
|
|
|
10X Tris-Tricine-SDS Buffer is used for polyacrylamide electrophoresis. Tris-Tricine-SDS Buffer is designed for the separation of small molecular weight proteins. The tris concentration is increased to a 0.1M solution, and the glycine is replaced with tricine. 10X Tris-Tricine-SDS Buffer can be used in denaturing polyacrylamide electrophoresis of proteins. Click on details to view Specification |
|
|
|
|
|
10X Tris-Tricine Buffer is used for polyacrylamide electrophoresis. Tris-Tricine Buffer is designed for the separation of small molecular weight proteins. The tris concentration is increased to a 0.1M solution, and the glycine is replaced with tricine. 10X Tris-Tricine Buffer can be used in denaturing polyacrylamide electrophoresis of proteins. Click on details to view Specification |
|
|
|
|
|
10X Tris-Tricine Buffer is used for polyacrylamide electrophoresis. Tris-Tricine Buffer is designed for the separation of small molecular weight proteins. The Tris concentration is increased to a 0.1M solution, and the glycine is replaced with Tricine. Tris-Tricine Buffer can be used in both native and denaturing (SDS) polyacrylamide gel electrophoresis of proteins. One pouch with produce approximately 1L of 10X Tris-Tricine Buffer Solution. Click on details to view Specification |
|
|
|
|
|
10X Tris-Tricine-SDS Buffer is used for polyacrylamide electrophoresis. Tris-Tricine- SDS Buffer is designed for the separation of small molecular weight proteins. The Tris concentration is increased to a 0.1M solution, and the glycine is replaced with Tricine. Tris- Tricine-SDS Buffer can be used in denaturing polyacrylamide electrophoresis of proteins. One pouch will produce approximately 1L of 10 Tris- Tricine-SDS Buffer Solution. Click on details to view Specification |
|
|
|
|
|
20X SSC Buffer is a solution formulated for use in nucleic acid preparation and blotting applications, including northern blotting. It is used in concentrations ranging from 0.2X to 20X, depending on the application. Click on details to view Specification |
|
|
|
|
|
20X SSPE Buffer is a solution formulated for use in nucleic acid hybridization applications. Click on details to view Specification |
|
|
|
|
|
IBI’s Ultra-Pure Grade 10X PBS solution is ideal for use in sample preparations and as a wash buffer in general immunoassay applications. 10X PBS also performs very well in tissue and cell culture procedures. IBI’s 10X PBS solution is a modified Dulbecco buffer that does not contain calcium or magnesium. Click on details to view Specification |
|
|
|
|
|
IBI’s Ultra-Pure Grade 10X PBS solution is ideal for use in sample preparations and as a wash buffer in general immunoassay applications. 10X PBS also performs very well in tissue and cell culture procedures. IBI’s 10X PBS solution is a modified Dulbecco buffer that does not contain calcium or magnesium. Click on details to view Specification |
|
| IBI Reagents - IBI Detergents | |
|
|
|
|
|
|
|
Triton X-100 is a non-ionic detergent used to denature cell membranes without denaturing the protein. Triton X-100 breaks up protein aggregates to promote enzymatic activity. Click on details to view Specification |
|
|
|
|
|
SDS is an ionic detergent used to denature proteins in hybridization, nucleic acid purification, and electrophoresis buffer systems. SDS is also used to dissociate nucleic acid protein complexes in DNA extraction protocols, to disrupt cell membranes and to prepare prehybridization and/or hybridization solutions. Click on details to view Specification |
|
|
|
|
|
SDS is an ionic detergent used to denature proteins in hybridization, nucleic acid purification, and electrophoresis buffer systems. SDS is also used to dissociate nucleic acid protein complexes in DNA extraction protocols, to disrupt cell membranes and to prepare prehybridization and/or hybridization solutions. Click on details to view Specification |
|
|
|
|
|
20% SDS Solution is an ionic detergent used to denature proteins in hybridization, nucleic purification, and electrophoresis buffer systems. SDS Solution is also used to dissociate nucleic acid protein complexes in DNA extraction protocols to disrupt cell membranes, and to prepare prehybridization and/or hybridization solutions. Click on details to view Specification |
|
|
|
|
|
Sarkosyl is an ionic detergent used to denature proteins in hybridization, nucleic acid purification, and electrophoresis. It is used in concentrated salt solutions as a detergent because SDS is insoluble in concentrated salt solutions. Click on details to view Specification |
|
|
|
|
|
NP-40 is a non-ionic detergent used to denature cell membranes without denaturing the protein. NP-40 detergent is also used to solubilize cerbral GABA receptors ans solubilization of proteins and lipids. Click on details to view Specification |
|
| IBI Reagents - IBI Dyes and Stains | |
|
|
|
|
|
|
|
Ethidium Bromide can be used to detect both single and double stranded nucleic acids (DNA and RNA). The recommended final concentration of Ethidium Bromide in an agarose gel and/or electrophoresis buffers is 0.5ug/ml. Click on details to view Specification |
|
|
|
|
|
Acridine Orange is a metochromatic stain that can be used to detect both single and double stranded nucleic acids. Click on details to view Specification |
|
|
|
|
|
Bromophenol Blue is used as a tracking dye to monitor the progress of electrophoresis separations. Click on details to view Specification |
|
|
|
|
|
Methylene Blue is a recommended stain for agarose gels when recovery of DNA is required. The benefit of using methylene blue is the ability to use a white light box for visualization and photography in place of a UV light box. Click on details to view Specification |
|
|
|
|
|
Ponceau S is a stain used to visualize proteins on microcellulose or PVDF membranes. Click on details to view Specification |
|
|
|
|
|
Xylene Cyanol FF is used as a tracking dye to monitor the progress of electrophoresis separations. The tracking dye typically migrates with the DNA molecules around 5kb. Therefore, if you are monitoring the progress of longer electrophoresis runs, Xylene Cyanol FF is the tracking dye of choice! Click on details to view Specification |
|
| IBI Reagents - IBI Loading Dyes | |
|
|
|
|
|
|
|
IBI 6X Loading Dye contains 15% ficoll in a special TRIS dye. It is ideal for DNA or RNA gels.This loading dye contains the three tracking dyes that make estimating sample migration easy and reliable. Click on details to view Specification |
|
|
|
|
|
IBI's 5X RNA Gel Loading Kit contains reagents for denaturing and loading RNA samples onto a formaldehyde gel, using MOPS as a buffer. The reagents are nuclease free and contain ultra pure deionized formamide and DEPC water. Click on details to view Specification |
|
|
|
|
|
IBI's 2X Protein Loading Dye helps track the migration progression of your sample during polyacrylamide electrophoresis. This loading dye not only gives color to the sample, but also increases the density to ensure efficient distribution in each well. IBI's loading dye migrates independently of the samples, making it easier to estimate the migration of proteins. Click on details to view Specification |
|
| IBI Reagents - IBI Molecular Biology Reagents | |
|
IBI Molecular Biology Certified Reagents have been satisfying the needs of molecular biologists for years. Our stringent quality control, convenient and safe product packaging, and complete product documentation provide you with the quality and convenience you expect from IBI products. Safety:Many of our IBI reagents are supplied in ready-to-use form that reduce your preparation time and exposure to potentially toxic chemicals. For maximum safety, we package hazardous materials in multi-layer packaging to prevent accidental exposure or breakage. All of our packaging meets DOT regulations for maximum safety and economical transport. Quality: All reagents meet stringent physical specifications, and then are functionally tested for performance in key applications. Examples of our functional tests include DNase and RNase, and protease tests. Results of both physical and functional tests as well as product use and guidelines are provided on the product label and on the certificate of analysis. |
|
|
|
|
|
IPTG is an inducer of B-galactosidase activity in E. coli. It is commonly used in conjunction with X-GAL to detect lac gene expression in cloning applications, thus allowing detection of recominant molecules. IBI offers IPTG in numerous sizes up to 25 grams for users that require larger quantities! Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IPTG is an inducer of B-galactosidase activity in E. coli. It is commonly used in conjunction with X-GAL to detect lac gene expression in cloning applications, thus allowing detection of recominant molecules. IBI offers IPTG in numerous sizes up to 25 grams for users that require larger quantities! Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IPTG is an inducer of B-galactosidase activity in E. coli. It is commonly used in conjunction with X-GAL to detect lac gene expression in cloning applications, thus allowing detection of recominant molecules. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IBI X-GAL is a histochemical substrate for B-galactosidase. X-GAL is a chromogenic stain for the detection of lac gene expression. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IBI X-GAL is a histochemical substrate for B-galactosidase. X-GAL is a chromogenic stain for the detection of lac gene expression. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
A primary component used in nucleic acid extraction procedures to aid in the complete removal of phenol from aqueous samples. Click on details to view Specification |
|
|
|
|
|
IBI provides redistilled crystalline phenol for use in nucleic acid purification. Click on details to view Specification |
|
|
|
|
|
IBI provides redistilled crystalline phenol for use in nucleic acid purification. Click on details to view Specification |
|
|
|
|
|
IBI provides phenol chloroform solution at a pH of 6.5 - 6.9 for use in typical DNA purification, at a 1:1 ratio. IBI's phenol chloroform solution is packaged at a standard pH of 6.7, but can be increased to 8.0 when mixed with supplied bottle of alkaline buffer. Click on details to view Specification |
|
|
|
|
|
IBI provides saturated phenol at a pH of 6.6 +/-0.1, for use in DNA purification. Included is a bottle of buffer for DNA applications that require a higher pH of 8.0. If your application does requier the addition of buffer, add the entire contents of the supplied buffer (6.5ml) to the saturated phenol stock. To use, allow the phases to separate and then add the appropriate amount of buffer saturated phenol to your DNA sample. Click on details to view Specification |
|
|
|
|
|
IBI provides saturated phenol at a pH of 4.3 +/- 0.2, for use in RNA purification. To use, allow the phases to separate and then add the appropriate amount of saturated phenol to your RNA sample. Click on details to view Specification |
|
|
|
|
|
IBI Proteinase K is a stable >50mg/ml (power) highly active proteolytic enzyme that is purified from the mold Tritrachium album. The enzyme has two binding sites for Ca++, which lie some distance from the active site, and is not directly involved in the catalytic mechanism. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IBI Proteinase K solution is a stable 20mg/ml highly active proteolytic enzyme that is purified>br> from the mold Tritirachium album. The enzyme has two binding sites for Ca++, which lie some distance from the active site and is not directly involved in the catalytic mechanism. Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
Guanidine HCl is an ionic denaturant that rapidly and effectively denatures most proteins. It is also used in the isolation of RNA. Click on details to view Specification |
|
|
|
|
|
Guanidine HCl Solution is an ionic denaturant that rapidly and effectively denatures most proteins. It is also used in the isolation of RNA. Click on details to view Specification |
|
|
|
|
|
Guanidine Thiocyanate is used in the isolation of RNA. Click on details to view Specification |
|
|
|
|
|
Formamide is used as a denaturant in hybridization and electrophoresis applications. Formamide is used to denature DNA and RNA, it separates the two sprands of the double helix. Click on details to view Specification |
|
|
|
|
|
Formamide is used as a denaturant in hybridization and electrophoresis applications. Formamide is used to denature DNA and RNA, it separates the two sprands of the double helix. Click on details to view Specification |
|
|
|
|
|
Blot Washing Formamide is suitable for blot washing procedures to remove background hybridization. Click on details to view Specification |
|
|
|
|
|
IBI provides technical grade Cesium Chloride for purification of DNA by density gradient centrifugation. Click on details to view Specification |
|
|
|
|
|
IBI provides optical grade Cesium Chloride for purification of DNA by density gradient centrifugation. Click on details to view Specification |
|
|
|
|
|
IBI provides optical grade Cesium Chloride for purification of DNA by density gradient centrifugation. Click on details to view Specification |
|
|
|
|
|
Glycerol is used to prevent freezing during enzyme and bacterial preparations. Click on details to view Specification |
|
|
|
|
|
Glycerol is used to prevent freezing during enzyme and bacterial preparations. Click on details to view Specification |
|
| IBI Reagents - IBI Premixed Dyes and Stains | |
|
|
|
|
|
|
|
IBI Blue-Clean Protein stain is a convenient alternative to traditional Coomassie Blue staining procedures. It. . . - Does NOT contain methanol or acetic acid. - Has sensitivity below 20ng of protein per/band. - Allows pre-wash and destain with DI water. - Is packaged as a 1X ready-to-use solution. - Will stain 40 gels (1L Bottle). IBI Blue Clean protein stain will reduce the amount of hazardous material your lab generates!! Click on details to view Specification Web Special: Please reference code web1009 |
|
|
|
|
|
IBI ethidium bromide can be used to detect both single stranded and double stranded nucleic acids (both DNA and RNA). However, ethidium bromide does not intercalate into single stranded DNA very well; therefore, the fluorescence of single stranded DNA is relatively poor in comparison to double stranded DNA. Click on details to view Specification |
|
|
|
|
|
SeeBand Protein Stain is a convenient alternative to traditional coomassie blue staining procedures. Environmentally friendly, this ready-to-use stain does not contain methanol or acetic acid, and does not require hazardous solvents for destaining. This simple "hands-off" staining/destaining procedure saves valuable time while reducing the handling of hazardous materials and solvent waste in your laboratory. Click on details to view Specification |
|
|
|
|
|
SeeBand Protein Stain is a convenient alternative to traditional coomassie blue staining procedures. Environmentally friendly, this ready-to-use stain does not contain methanol or acetic acid, and does not require hazardous solvents for destaining. This simple "hands-off" staining/destaining procedure saves valuable time while reducing the handling of hazardous materials and solvent waste in your laboratory. Click on details to view Specification |
|
|
|
|
|
IBI's Silver Stain Kit is a rapid and easy-to- use method to achieve excellent silver staining of nucleic acids or proteins in polyacrylamide gels. IBI Silver Stain has outstanding sensitivity with very low background. This kit provides sufficient , pre-measured reagents for staining 20 gels. IBI Silver Stain kit contains the following: 1. 10X Sensitizer Solution 2. 10X Silver Stain solution 3. 5X developer solution Click on details to view Specification |
|
| IBI Reagents - IBI Protease Inhibitors | |
|
|
|
|
|
|
|
An irreversible serine protease inihibitor of trypsin, chymotrypsin, kallikrein, subtilisin, and thrombin, as well as cysteine preotease papain. Working Range: 0.1 - 1.0mM 0.2 Soluble in Ethanol and Methanol Click on details to view Specification |
|
|
|
|
|
Protease Inhibitor Cocktails are an easy-to-use lypophilized power. Add 1ml of ddi water to the vial and mix gently. The reconstituted protease cocktail should be aliquoted into multiple tubes and frozen. This material can be stored up to two weeks. A 1ml vial of protease cocktail is sufficient for 100ml of sample buffer. Click on details to view Specification |
|
|
|
|
|
Protease Inhibitor Cocktail w/EDTA is an easy-to-use lyophilized power. Add 1ml of ddi water to the vial and mix gently. The constituted protease cocktail w/EDTA should be aliquoted into multiple tubes and frozen. This material can be stored up to two weeks. A 1ml vial of protease cocktail is sufficient for 100ml of sample buffer. Click on details to view Specification |
|
| IBI Reagents - IBI Protein Markers | |
|
|
|
|
|
|
|
IBI's Molecular Weight Protein Markers recombinate 7 proteins that are spaced at convenient intervals for easy identification. The 7 bands; 15, 25, 35, 50, 75, 100, and 150kDa provide an exact banding pattern for accurate molecular weight determination of unknown protein samples. The protein markers provide an accurate "ladder-like" array. Click on details to view Specification |
|
|
|
|
|
IBI's Molecular Weight Protein Markers are designed for the determination of approximate molecular weights of proteins by SDS polyacrylamide electrophoresis. The protein markers are a mixture of purified proteins of known molecular weights, supplied in ready-to-use loading buffer (contains aside). These high range markers will give 5 protein bands; from 200,000 to 39,200kDa. Click on details to view Specification |
|
| IBI Reagents - IBI Protein Purification | |
|
|
|
|
|
|
|
IBI's Bradford Protein Assay Kit is based on a complex formation between basic and aromatic amino acid residues with coomassie blue stain. The protocol can measure 1 to 10ug of protein and the kit comes complete with 0.5mg/ml BSA standard solution. Click on details to view Specification |
|