PCDH15 Mouse Monoclonal Antibody [Kloon ID: LBI7F10]

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]

Carrier-free (BSA/glycerol-free) PCDH15 mouse monoclonal antibody, clone LBI7F10

CDHR15; DFNB23; USH1F

Homo sapiens protocadherin related 15 (PCDH15), transcript variant A, mRNA.

65217

Q96QU1

Unconjugated

WB 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome, Transmembrane

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

PCDH15

https://www.ncbi.nlm.nih.gov/gene/?term=65217

https://www.uniprot.org/uniprot/Q96QU1