Life Science Buffers
Balanced salt solutions and powders used for molecular, protein, nucleic acid, and cell biology applications including cell culture, electrophoresis, ELISA, and chromatography processes; available in a variety of formulations and grades.
Buffer solutions serve to keep pH (acidity or alkalinity) nearly constant in a variety of chemical and biological applications. For example, a bicarbonate buffer helps maintain the pH of blood, a buffered saline maintains cellular contents at a consistent pH level, and buffers help maintain a narrow pH range for enzymes to function correctly.
Most biological samples used in research are kept at a pH of about 7.4. Common biological buffers used for tissue culture include Dulbeccos phosphate buffered saline (PBS), Tris base, HEPES, MOPS, PIPES, and other formulations developed for specific cell lines or applications. Most buffers used in cell culture are also DNase-, RNase-, and protease-free.
The choice of buffer for a particular biological reaction or site depends on several factors:
- Temperature
- Desired or target pH
- Buffer toxicity (to the system)
- Buffer interactions with other system components
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Filtered Search Results
VWR INTERNATIONAL LLC Phosphate Buffered Saline (PBS) 20X, Ultra Pure Grade
1X Solution Composition:135 mM NaCl, 2.7 mM KCl,11 mM Phosphate Buffer. Does not contain magnesium or calcium.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Boston Bioproducts Inc Tris-HCl Buffer (1 M, pH 9.5) - 1L
The Tris-HCl Buffer is a widely used bufering reagent in molecular biology and biochemistry, acting to maintain a stable pH, and preserve the integrity of target macromolecules. The buffering capacity of Tris-HCl is effective in the pH range of 7.0 to 9.0, making it ideal for many biological applications like cell culture, molecular biology, DNA/RNA extraction, electrophoresis, enzyme assays and immunohistostaining.
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Bio Rad Laboratories 10X TRIS GLYCINE 5LTR
10x Tris Glycine 6x1ltr
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HORIZON DISCOVERY BIOSCIENCES LIMITED 10MM TRIS-HCL BUFFER PH 7.4
NC2372517 10MM TRIS-HCL BUFFER PH 7.4
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SANTA CRUZ BIOTECHNOLOGY TBST 10X LIQUID
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NC9529580 TBST 10X LIQUID
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Teknova 1M HEPES, pH 7.0. 1000mL, Sterile
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HEPES solution is a Goods buffer that is commonly used in cell culture and biochemical applications. It is well known for its ability to maintain pH level, making it an essential part of any experiment that requires a stable pH. It has a buffering range of 6.8 - 8.2.
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GENSCRIPT USA INCORPORATED SUREPAGE BIS-TRIS 10X8 4-10X8
NC2951982 SUREPAGE BIS-TRIS 10X8 4-10X8
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Biolegend Annexin V Binding Buffer, 100 mL
Annexin V Binding Buffer Apps: FC, IF; Size: 100 mL
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Cell Signaling Technology Tris Buffered Saline (TBS-10X) 1 liter
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Tris Buffered Saline (TBS-10X) 1 liter
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Thomas Scientific 10X PBS SOLUTION 4L
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10x PBS Solution (Phosphate Buffered Saline), 4L
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Teknova 1M Tris-HCl, pH 8.0. 1000mL, Sterile, Endotoxin Tested, PCR Grade.
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Tris (tris(hydroxymethyl)aminomethane) is used as a component ofbuffer solutions, especially for solutions ofnucleic acids. The useful buffer range for tris (pH 7–9) is similar to the pH of most living organisms. This, and its low cost, make tris one of the most common buffers in the biology/biochemistry laboratory.
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Abcam Mammalian Cell Lysis Buffer 5X (ab179835)
Mammalian Cell Lysis Buffer 5X (ab179835)
The product is subject to the following: Abcam Restricted Use Statement
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Bioworld EGTA 0.5M, pH 8.0, DNase and RNase Free, 50 mL
EGTA Buffer is of a 0.5M concentration and pH of 8.0 that is DNase and RNase free. EGTA Buffer is a metal chelating agent specific for calcium ions. EGTA Buffer is commonly used in tissue culture media and biological buffers.
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NOVATEIN BIOSCIENCES TRIS-ACETATE BUFFER 1M PH 8.
NC1127118 TRIS-ACETATE BUFFER 1M PH 8.
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Supply Solutions Red Blood Cell Lysing Buffer Hybri-Max™, 100mL
Recommended for use by adding 1 mL of buffer to a cell pellet (cell pellet = 1 spleen or 100-200 million cells). Gently mix for 1 minute. Dilute the buffer with 15-20 mL of medium or salt solution. Centrifuge at 250-500 g for 7 minutes and decant the supernatant. Cells may be diluted and prepared for counting or fusion. If lysis is incomplete, steps 1-4 may be repeated.
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