PCDH15 Antibody
Product Specifications
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.
NCBI Gene ID
65217
Swiss Prot
Q96QU1
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 160-400 of human PCDH15 (NP_001136235.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Other
Purification
Affinity purification
Positive Control
SH-SY5Y
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 100kDa
Fragment
IgG
Symbol
PCDH15
Positive Control 2
293T
Positive Control 3
A-549
Positive Control 4
Raji
Positive Control 5
Mouse brain
Positive Control 6
Mouse liver
NCBI Official Name
Protocadherin-related 15
NCBI Organism
Homo sapiens
Other Product Names
PCDH15, RP11-449J3.2, DFNB23, DKFZp667A1711, USH1F, CDHR15
Tested Applications
WB, IHC
Physical Properties
Liquid
Curated Selection
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