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Fish Gelatin Powder

Gelatin from fish skin that can be added to blocking buffers to minimize non-specific antibody binding in immuno-detection procedures such as western blotting and cell staining.

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2 x 50 g
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Product Description

Fish Gelatin Powder is purified from cold water fish skin. It can be used to make blocking buffers to minimize non-specific antibody binding in immunodetection procedures such as western blotting, immunofluorescence, and IHC.

  • Gelatin purified from cold water fish skin
  • Blocking agent for immuno-assays (ie, western blot, IHC, IF)
  • Minimizes non-specific antibody binding
  • Contains no IgG or serum proteins, won’t cross-react with mammalian antibodies
  • 2 x 50g of solid gelatin
  • Store solid at room temperature

Fish gelatin can be used to block non-specific binding sites on positively charged nylon or PVDF membranes or used for blocking and dilution of antibodies during immunostaining procedures. Unlike BSA or milk, fish gelatin does not contain IgG or serum proteins that could cross-react with mammalian antibodies.

Product Attributes

Size
2 x 50 g
Storage Conditions
Store at room temperature

Documents, Protocols, SDS and COA

References

1. Oncotarget (2017) Sep 28;8(49):86657-86670 doi:10.18632/oncotarget.21364
2. Heliyon (2018) Nov 16;4(11):e00917 doi:10.1016/j.heliyon.2018.e00917
3. Exp Eye Res (2019) Mar;180:122-128 doi:10.1016/j.exer.2018.12.016
4. Environ Mol Mutagen (2020) Feb;61(2):235-245 doi:10.1002/em.22331

Citations

1. Oncotarget (2017) Sep 28;8(49):86657-86670 doi:10.18632/oncotarget.21364
2. Heliyon (2018) Nov 16;4(11):e00917 doi:10.1016/j.heliyon.2018.e00917
3. Exp Eye Res (2019) Mar;180:122-128 doi:10.1016/j.exer.2018.12.016
4. Environ Mol Mutagen (2020) Feb;61(2):235-245 doi:10.1002/em.22331

FAQs

Protein Detection & Analysis

Even though AccuOrange™ buffer does contain SDS, which is required for the dye to bind proteins, the assay is very sensitive to small changes in SDS concentration, and also cannot tolerate non-ionic detergents that form mixed micelles with SDS, like Triton®. Therefore we don’t recommend using the kit for cell lysates or other samples with significant amounts of detergents.

Gels stained with One-Step Blue® can be dried just like gels stained with Coomassie. The stain will not interfere with the detection of radiolabeled proteins.

The AccuOrange™ assay is a fluorescent dye-based assay. The dye binds to proteins primarily through hydrophobic interactions. Proteins denature upon heating; the dye binds to the exposed hydrophobic pockets of the protein after cooling. The free AccuOrange™ dye is fluorogenic due to non-radioactive decay but becomes highly fluorescent due to the rigid conformation inside the pocket.

The AccuOrange™ assay more sensitive than traditional protein quantitation assays such as BCA, Bradford and Lowry, and shows superior linearity and reproducibility than the NanoOrange® protein quantitation assay (Thermo Fisher Sci.), but has low tolerance for detergents like SDS and Triton® X-100.

 

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