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BCIP, Na

A water soluble formulation of the most widely used chromogenic phosphatase substrate for the detection of alkaline phosphatase labeled proteins in a variety of applications, such as immunohistochemistry, westerns, and in situ hybridization.

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100 mg
500 mg
5 g
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Product Description

BCIP (5-Bromo-4-chloro-3-indoxyl phosphate) is the most widely used chromogenic phosphatase substrate, which forms a dark blue (λmax 615 nm) precipitate on enzymatic hydrolysis. It is often used with the oxidant NBT (nitro blue tetrazolium chloride, 10008), which facilitates the precipitation, to detect alkaline phosphatase-activity and -labeled proteins in a variety of applications, such as immunohistochemistry, westerns, and in situ hybridization.

  • Colormetric detection of alkaline phosphatase activity and labels
  • Compatible with a variety of  applications
  • Use alone or in combination with NBT
  • White solid soluble in water

For your convenience, we offer a  BCIP/NBT Kit (10003)  that contains both reagents. We also offer Alkaline Phosphatase Conjugated Antibodies.

Find the Right Stain for your Application

The original BCIP forms a dark blue (λmax 615 nm) precipitate and is available in two different salt formulations; BCIP, toluidine salt is soluble in DMF while BCIP, sodium salt is soluble in water. We also offer a Pink BCIP derivative, which produces a pink colored (λmax 540 nm) precipitate. BCIP Red produces a red colored (λmax 565 nm) precipitate. Please see our BCIP Kits that are paired with NBT (nitro blue tetrazolium chloride) for user convenience.

Molecular Structure:

Product Attributes

Size
100 mg, 500 mg, 5 g
CAS number
102185-33-1
Molecular weight
370.5
Storage Conditions
Store at 2 to 8 °C or below, Protect from light, Desiccate

Documents, Protocols, SDS and COA

References
  1. Histochemistry 58, 203 (1978), DOI: 10.1007/bf00495720
  2. Biotechniques 12, 656 (1992), PMID: 1381193
  3. Dev. Dyn., 240, 589 (2011), DOI: 10.1002/dvdy.22544
  4. Dev Comp Immunol. 65, 41 (2016), DOI: 10.1016/j.dci.2016.06.017
  5. Molecular Medicine Reports 15, 1455 (2017), DOI: 10.3892/mmr.2017.6162

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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