Recombinant P-Cadherin antibody (PE)

Catalog No. ABIN7867396

The PE-conjugated Rabbit Chimeric anti-P-Cadherin antibody (Clone 6A10) (ABIN7867396) specifically detects P-Cadherin in FACS. The antibody is reactive with Human samples.

Quick Overview for Recombinant P-Cadherin antibody (PE) (ABIN7867396)

Target: P-Cadherin (CDH3)

Antibody Type: Recombinant Antibody

Reactivity: Human

Host: Rabbit

Clonality: Chimeric

Conjugate: This P-Cadherin antibody is conjugated to PE

Application: Flow Cytometry (FACS)

Clone: 6A10

Product Details anti-P-Cadherin Antibody (PE)

Purpose: PE-conjugated Anti-CDH3 antibody(6A10), IgG1 Chimeric mAb

Purification: Purified from cell culture supernatant by affinity chromatography

Isotype: IgG1

Application Details

Application Notes: Flow Cyt 1:100

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid PBS with 0.05 %  Proclin300, 1 % BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C

Storage Comment: Store at 2°C-8°C for 6 months

Expiry Date: 6 months

Target Details for P-Cadherin

Target: P-Cadherin (CDH3)

Alternative Name: CDH3

Background:

Synonyms: CDHP,HJMD,PCAD

Target Background: This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas. Mutations in this gene are associated with hypotrichosis with juvenile macular dystrophy and ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome (EEMS). [provided by RefSeq, Nov 2015]

UniProt: P22223