Applications: Suitable for product packaging and storage requirements in molecular biology and cell biology, laboratory medicine, genomics and proteomics and other areas. Product Features The raw materials, premium polypropylene (PP)/polyethylene (HDPE), have excellent physical and chemical indicators, pressure-resistance, impact-resistance, and acid and alkali resistance. PP materials can undergo autoclave sterilization at 121°C; HDPE can be stored at -80°C. Pre-washed/Ready-to-use: no need for tedious pre-cleaning Thickened middle packaging to ensure transportation and storage safety. Use of professional leak-proof design for bottle mouth, with no need for inner cover or inner gasket for protection, excellent sealability. 100% leak-proof to ensure safety even during air transportation; wide-mouthed design for easy access of liquid. No biotoxicity, pyrogen-free, DNAse/RNAse-free, manufactured in a 100-thousand grade clean plant. Sterilized using GAMMA-ray. Using automated production equipment, the bottles have fine details and evenly glossed walls. In addition, batches are incredibly uniform.  By using high-grade molding and surface processing technologies, the bottles feature smooth interior and exterior surfaces that prevent the wicking effect of reagents, thereby significantly reducing sample wastage SKU Volume (ml) Material Color Bottles per Bag Total Bottles 336101 15 HDPE Natural 20 400 337101  30 HDPE Natural 10 200 338101 60 HDPE Natural 10 200 339101 125 HDPE Natural 10 100 340101 250 HDPE Natural 10 100 341101 500 HDPE Natural 5 50

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6X DNA Loading Buffer is a Ficoll 400-based ready-to-use DNA loading dye for tracking DNA migration during electrophoresis. it contains three dyes with different migration pattern: xylene cyanol FF migrates at approximately 4kb (Blue), bromophenol blue at 300bp (Purple) and orange G at 50bp (Orange) on a 1% agarose gel. Storage: Room temperature or 4 °C

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6X DNA Loading Buffer is a Ficoll 400-based ready-to-use DNA loading dye for tracking DNA migration during electrophoresis. 6X DNA Loading Buffer contains three dyes with different migration pattern: xylene cyanol FF migrates at approximately 4kb (Blue), bromophenol blue at 300bp (Purple) and orange G at 50bp (Orange) on a 1% agarose gel. Storage: Room temperature or 4 °C MSDS

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Ethium bromide replacement! 6xFluorescent DNA Loading Dye is formulated by mixing fluorescent dye with standard DNA loading dye and is used by adding to DNA samples directly. There is no need to add safe DNA gel stain or other fluorescent dye to the gel or running buffer. After the electrophoresis, the green DNA bands could be viewed under UV light or LED blue light.  Specifications Storage Store at 4 °C. Shelf life Two years from date of shipping. Safety Non-carcinogenic by the ames test. May cause skin and eye irritation. Always wear gloves when working with the product. Disposal Dispose as you  would any other non-carcinogenic fluorescent dye (eg. Acridine orange; Propidium iodide).   Protocol Prepare a 100 ml agarose or polyacrylamide solution with no stain. Mix gently to avoid bubbles. For agarose gels, let the solution cool down to 60 - 70 oC before casting the gel. For polyacrylamide gel, add APS and TEMED and cast the gel according to regular protocol. Mix samples or DNA marker with SafeRed dye at a 1:5 (dye : sample) dilution rate.  Following electrophoresis, view the results under UV and LED blue light. 

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Ethium bromide replacement! 6xFluorescent DNA Loading Dye is formulated by mixing fluorescent dye with standard DNA loading dye and is used by adding to DNA samples directly. There is no need to add safe DNA gel stain or other fluorescent dye to the gel or running buffer. After the electrophoresis, the green DNA bands could be viewed under UV light or LED blue light.  Specifications Storage Store at 4 °C. Shelf life Two years from date of shipping. Safety Non-carcinogenic by the ames test. May cause skin and eye irritation. Always wear gloves when working with the product. Disposal Dispose as you  would any other non-carcinogenic fluorescent dye (eg. Acridine orange; Propidium iodide).   Protocol Prepare a 100 ml agarose or polyacrylamide solution with no stain. Mix gently to avoid bubbles. For agarose gels, let the solution cool down to 60 - 70 oC before casting the gel. For polyacrylamide gel, add APS and TEMED and cast the gel according to regular protocol. Mix samples or DNA marker with SafeRed dye at a 1:5 (dye : sample) dilution rate.  Following electrophoresis, view the results under UV and LED blue light. 

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Ethium bromide replacement! 6x Red Fluorescent DNA Loading Dye is formulated by mixing fluorescent dye with standard DNA loading dye and is used by adding to DNA samples directly. There is no need to add safe DNA gel stain or other fluorescent dye to the gel or running buffer. After the electrophoresis, the red DNA bands could be viewed under UV light. Specifications Storage Store at 4 °C. Shelf life Two years from date of shipping. Safety Non-carcinogenic by the ames test. May cause skin and eye irritation. Always wear gloves when working with the product. Disposal Dispose as you  would any other non-carcinogenic fluorescent dye (eg. Acridine orange; Propidium iodide).   Protocol Prepare a 100 ml agarose or polyacrylamide solution with no stain. Mix gently to avoid bubbles. For agarose gels, let the solution cool down to 60 - 70 oC before casting the gel. For polyacrylamide gel, add APS and TEMED and cast the gel according to regular protocol. Mix samples or DNA marker with SafeRed dye at a 1:5 (dye : sample) dilution rate.  Following electrophoresis, view the results under UV. 

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Ethium bromide replacement! 6x Red Fluorescent DNA Loading Dye is formulated by mixing fluorescent dye with standard DNA loading dye and is used by adding to DNA samples directly. There is no need to add safe DNA gel stain or other fluorescent dye to the gel or running buffer. After the electrophoresis, the red DNA bands could be viewed under UV light. Specifications Storage Store at 4 °C. Shelf life Two years from date of shipping. Safety Non-carcinogenic by the ames test. May cause skin and eye irritation. Always wear gloves when working with the product. Disposal Dispose as you  would any other non-carcinogenic fluorescent dye (eg. Acridine orange; Propidium iodide).   Protocol Prepare a 100 ml agarose or polyacrylamide solution with no stain. Mix gently to avoid bubbles. For agarose gels, let the solution cool down to 60 - 70 oC before casting the gel. For polyacrylamide gel, add APS and TEMED and cast the gel according to regular protocol. Mix samples or DNA marker with SafeRed dye at a 1:5 (dye : sample) dilution rate.  Following electrophoresis, view the results under UV. 

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DescriptionTris-Glycine Native Sample Buffer (6x) is used to prepare protein samples for native gel electrophoresis using Tris-Glycine gels or Tris-Acetate gels. It has a pH of 6.8 and contains bromophenol blue as a tracking dye.To use: Heat the sample in a 1X dilution (reduced or non-reduced) at 85°C for 2–5 minutes for optimal results.Note: Heating samples at 100°C in SDS-containing buffers results in proteolysis.Composition: 600mM Tris.HCl, 50% glycerol, 0.02% bromophenol blue (Non-reduced). Add ß-mercaptoethanol (9% V/V) before use (Reduced).

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Description Tris-Glycine Native Sample Buffer (6x) is used to prepare protein samples for native gel electrophoresis using Tris-Glycine gels or Tris-Acetate gels. It has a pH of 6.8 and contains bromophenol blue as a tracking dye. To use: Heat the sample in a 1X dilution (reduced or non-reduced) at 85°C for 2–5 minutes for optimal results. Note: Heating samples at 100°C in SDS-containing buffers results in proteolysis. Composition: 600mM Tris.HCl, 50% glycerol, 0.02% bromophenol blue (Non-reduced). Add ß-mercaptoethanol (9% V/V) before use (Reduced).

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Tris-Glycine SDS Sample Buffer (6x) is used to prepare protein samples for denaturing gel electrophoresis using Tris-Glycine gels. It has a pH of 6.8 and contains bromophenol blue as a tracking dye.To use: Heat the sample in a 1X dilution (reduced or non-reduced) at 85°C for 2–5 minutes for optimal results. Note: Heating samples at 100°C in SDS-containing buffers results in proteolysis. Composition: 375 mM Tris.HCl, 9% SDS, 50% glycerol, 0.015% bromophenol blue (Non-reduced). Add ß-mercaptoethanol (9% V/V) before use (Reduced). MSDS

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Tris-Glycine SDS Sample Buffer (6x) is used to prepare protein samples for denaturing gel electrophoresis using Tris-Glycine gels. It has a pH of 6.8 and contains bromophenol blue as a tracking dye.To use: Heat the sample in a 1X dilution (reduced or non-reduced) at 85°C for 2–5 minutes for optimal results. Note: Heating samples at 100°C in SDS-containing buffers results in proteolysis. Composition: 375 mM Tris.HCl, 9% SDS, 50% glycerol, 0.015% bromophenol blue (Non-reduced). Add ß-mercaptoethanol (9% V/V) before use (Reduced). MSDS

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70µm Cell Strainer. Nylon mesh and compatible with 50ml Centrifuge Tubes. Features a polypropylene frame with a molded tab for easy handling. Gamma radiation sterilized, non-pyrogenic, and individually wrapped. Orange, 100 pieces/case. Features Strong nylon mesh for optimal performance in a variety of applications  Evenly spaced mesh pores providing consistent and reliable results  Polypropylene frame features a molded tab for easy handling  Conveniently accessible in individual packaging with gamma radiation Fits perfectly into 50 ml conical Centrifuge Tubes Different colors for optimum sample organization 

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