Recombinant P-Cadherin anticorps (PE)

N° du produit ABIN7867396

Cet anticorps anti-P-Cadherin Chimeric Lapin conjugué à PE (Clone 6A10) (ABIN7867396) détecte spécifiquement P-Cadherin dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Recombinant P-Cadherin anticorps (PE) (ABIN7867396)

Antigène: P-Cadherin (CDH3)

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Lapin

Clonalité: Chimeric

Conjugué: Cet anticorp P-Cadherin est conjugé à/à la PE

Application: Flow Cytometry (FACS)

Clone: 6A10

Détail du produit anti-P-Cadherin anticorps (PE)

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

Purification: Purified from cell culture supernatant by affinity chromatography

Isotype: IgG1

Information d'application

Indications d'application: Flow Cyt 1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C

Stockage commentaire: Store at 2°C-8°C for 6 months

Date de péremption: 6 months

Détails sur P-Cadherin

Antigène: P-Cadherin (CDH3)

Autre désignation: CDH3

Sujet:

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