PCDH15 polyclonal, anti-human, mouse, rat

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.

Synonyms: CDHR15, DFNB23, USH1F

Cellular Location: Cell membrane Secreted Single-pass type I membrane protein

Immunogen:
Recombinant protein of human PCDH15

Gene Symbol: PCDH15

Gene ID: 65217

Swiss prot: Q96QU1

Calculated MW: 216kDa

Recommended dilution:
WB 1:500-2000

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.