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0.5M EDTA pH 8.0, disodium EDTA 2H2O 186.12 g/L, sufficient NaOH to adjust pH 8.0
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0.5M EDTA pH 8.0, disodium EDTA 2H2O 186.12 g/L, sufficient NaOH to adjust pH 8.0
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0.5M EDTA pH 8.0, disodium EDTA 2H2O 186.12 g/L, sufficient NaOH to adjust pH 8.0
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LB Agar Plates are used for the growth and maintenance of E. coli strains used in molecular microbiology procedures.
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LB Agar Plates are used for the growth and maintenance of E. coli strains used in molecular microbiology procedures.
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100mg/ml Ampicillin Ready-Made Solution. 0.2µm filtered. Broad spectrum antibiotic that inhibits cell wall synthesis in gram-negative & gram-positive bacteria.
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Minimum Non-Essential Amino Acids [100X]are frequently used in Cell Biology research. The following are examples where MEM-NEAA 100X may be usefully employed: To maintain cell culture growth; To study cellular protein metabolism. DIRECTIONS: Dilute the Minimum Non-Essential Amino Acids [100X] one hu..
Minimum Non-Essential Amino Acids [100X]are frequently used in Cell Biology research. The following are examples where MEM-NEAA 100X may be usefully employed: To maintain cell culture growth; To study cellular protein metabolism. DIRECTIONS: Dilute the Minimum Non-Essential Amino Acids [100X] one hu..
10X Dulbecco’s Phosphate Buffered Saline without Calcium & Magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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Dulbecco’s Phosphate Buffered Saline without Calcium & Magnesium is frequently used as a reagent (“wash buffer”) in Cell Biology. The following are examples where PBS without Calcium & Magnesium may be usefully employed: “Wash buffer” for cell culture when perfo..
10X Dulbecco’s Phosphate Buffered Saline without Calcium & Magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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Dulbecco’s Phosphate Buffered Saline without Calcium & Magnesium is frequently used as a reagent (“wash buffer”) in Cell Biology. The following are examples where PBS without Calcium & Magnesium may be usefully employed: “Wash buffer” for cell culture when perfo..
10X Phosphate Buffered Saline pH 7.2, without calcium & magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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Phosphate Buffered Saline pH 7.4 is frequently used as a “wash buffer” or reagent in both Cell Biology and Molecular Biology techniques. The following are examples where Phosphate Buffered Saline pH 7.4 may be usefully employed: “Wash buffer” for cell culture when performing ..
10X Phosphate Buffered Saline pH 7.4, without calcium & magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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10X Phosphate Buffered Saline pH 7.4, without calcium & magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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10X Phosphate Buffered Saline pH 7.4, without calcium & magnesium, prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy and all sizes have been sterility tested.
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Phosphate Buffered Saline pH 7.4 is frequently used as a “wash buffer” or reagent in both Cell Biology and Molecular Biology techniques. The following are examples where Phosphate Buffered Saline pH 7.4 may be usefully employed: “Wash buffer” for cell culture when performing ..
Phosphate Buffered Saline pH 7.4 is frequently used as a “wash buffer” or reagent in both Cell Biology and Molecular Biology techniques. The following are examples where Phosphate Buffered Saline pH 7.4 may be usefully employed: “Wash buffer” for cell culture when performing ..
Phosphate Buffered Saline pH 7.4 is frequently used as a “wash buffer” or reagent in both Cell Biology and Molecular Biology techniques. The following are examples where Phosphate Buffered Saline pH 7.4 may be usefully employed: “Wash buffer” for cell culture when performing ..
This MOPS-containing RNA Gel Buffer is employed for electrophoresis of RNA through denaturing gels containing formaldehyde.
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10X RNA Gel Loading Solution. Treated with diethylpyrocarbonate (DEPC) to inactivate ribonucleases. Bromophenol blue 0.25% (w/v) 2.5 g/L, xylene cyanole FF 0.25% (w/v) 2.5 g/L, disodium EDTA 2H2O 0.37 g/L 1mM, glycerol 50% (v/v) 500ml.
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10X RNA Gel Loading Solution. Treated with diethylpyrocarbonate (DEPC) to inactivate ribonucleases. Bromophenol blue 0.25% (w/v) 2.5 g/L, xylene cyanole FF 0.25% (w/v) 2.5 g/L, disodium EDTA 2H2O 0.37 g/L 1mM, glycerol 50% (v/v) 500ml.
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Both TAE and TBE Buffers are widely used for DNA electrophoresis. However, TAE Buffer may be more suitable for electrophoresis if DNA is to be recovered from the agarose and purified using commercially available DNA purification kits.
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Both TAE and TBE Buffers are widely used for DNA electrophoresis. However, TAE Buffer may be more suitable for electrophoresis if DNA is to be recovered from the agarose and purified using commercially available DNA purification kits. Prepared using water deionized by Reverse Osmosis, 0.1µm st..
Because of its high buffering capacity, TBE Buffer is routinely used at a 1X concentration for DNA electrophoresis involving extended periods of time or high voltages. When used for DNA electroelution from gel slices or electrophoresis onto DEAD cellulose membrane, TBE should be diluted to 0.5X fir ..
Because of its high buffering capacity, TBE Buffer is routinely used at a 1X concentration for DNA electrophoresis involving extended periods of time or high voltages. When used for DNA electroelution from gel slices or electrophoresis onto DEAD cellulose membrane, TBE should be diluted to 0.5X fir ..
 STERILE_4L_351-001-491-80x80.jpg "10X TBE (MBG) 4L, (351-001-491) QBIC20075 Quality Biological")
Because of its high buffering capacity, TBE Buffer is routinely used at a 1X concentration for DNA electrophoresis involving extended periods of time or high voltages. When used for DNA electroelution from gel slices or electrophoresis onto DEAD cellulose membrane, TBE should be diluted to 0.5X fir ..
Because of its high buffering capacity, TBE Buffer is routinely used at a 1X concentration for DNA electrophoresis involving extended periods of time or high voltages. When used for DNA electroelution from gel slices or electrophoresis onto DEAD cellulose membrane, TBE should be diluted to 0.5X fir ..
Tris HCl 31.52 g/L 0.2M; NaCl 87.66 g/L 1.5M; sufficient NaOH to adjust to pH 7.2 DNase, RNase tested. Store at: 15-30°C, Shipped: at ambient temperature
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10X TBS pH 7.4 (Tris Buffered Saline). Tris base 30.28 g/L 0.25M, NaCl 80.06 g/L 1.37M, KCl 2.24 g/L 0.03M, sufficient HCL to adjust to pH 7.4.
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10X TBS pH 7.4 (Tris Buffered Saline), prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy.
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10X TBS pH 7.4 (Tris Buffered Saline), prepared using water deionized by Reverse Osmosis, 0.1µm sterile filtered. Cube containers have been gamma irradiated to a minimum of 25kGy and a maximum of 50kGy.
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10X TBS pH 7.4 (Tris Buffered Saline). Tris base 30.28 g/L 0.25M, NaCl 80.06 g/L 1.37M, KCl 2.24 g/L 0.03M, sufficient HCL to adjust to pH 7.4.
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10X TBS pH 7.4 (Tris Buffered Saline). Tris base 30.28 g/L 0.25M, NaCl 80.06 g/L 1.37M, KCl 2.24 g/L 0.03M, sufficient HCL to adjust to pH 7.4.
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10X TBS pH 7.4 (Tris Buffered Saline). Tris base 30.28 g/L 0.25M, NaCl 80.06 g/L 1.37M, KCl 2.24 g/L 0.03M, sufficient HCL to adjust to pH 7.4.
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10X Tris Glycine Transfer Buffer, at a 1X concentration with the addition of 20% methanol, is used for electrophoretic transfer of proteins from denaturing polyacrylamide gel to a solid membrane support (western blotting).
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HEPES is frequently used in cell culture media as a buffer alternative to the more traditional sodium bicarbonate (NaHCO3). HEPES is a very strong buffer within the pH range of7.2-7.6. DIRECTIONS: Dilute the HEPES 1M, pH 7.3 in the appropriate cell culture medium. Typically, HEPES is diluted to a fi..
HEPES is frequently used in cell culture media as a buffer alternative to the more traditional sodium bicarbonate (NaHCO3). HEPES is a very strong buffer within the pH range of7.2-7.6. DIRECTIONS: Dilute the HEPES 1M, pH 7.3 in the appropriate cell culture medium. Typically, HEPES is diluted to a fi..
1M TRIS HCl pH 7.5. Tris base 121.14 g/L, sufficient HCL to adjust to pH 7.5
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1M TRIS HCl pH 7.5. Tris base 121.14 g/L, sufficient HCL to adjust to pH 7.5
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1M TRIS HCl pH 7.5. Tris base 121.14 g/L, sufficient HCL to adjust to pH 7.5
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