PCDH15 Antilichaam

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.

65217

Q96QU1

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1) .

Unconjugated

Primary Antibodies

Other

Affinity purification

SH-SY5Y

Batch dependent

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

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 100kDa

IgG

PCDH15

293T

A-549

Raji

Mouse brain

Mouse liver

Protocadherin-related 15

Homo sapiens

PCDH15, RP11-449J3.2, DFNB23, DKFZp667A1711, USH1F, CDHR15

WB, IHC

Liquid