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PCDH15 monoclonal Antibody | MB64379

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BW-MB64379
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Description

PCDH15 monoclonal Antibody | MB64379 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human, Mouse, Rat

Application: WB

Application Range: WB 1:500

Background: This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F) . Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]

Storage & Stability: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Specificity: protocadherin-related 15

Molecular Weight: 217.06 kDa (Predicted)

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: CDHR15; DFNB23; USH1F

Immunogen: Human recombinant protein fragment corresponding to amino acids 160-400 of human PCDH15 (NP_001136235) produced in E.coli.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Pathway: N/A

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