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Anti-P-Cadherin Antibody

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Description: Rabbit polyclonal antibody to P-Cadherin.
Category: Primary Antibodies
Applications: WB, IHC, FC
Host: Rabbit
Clonality: Polyclonal
Isotype: IgG
Reactivity: Human
UniProt: P22223
Gene ID: 1001
Immunogen: A synthetic peptide of human CDH3
Protein Length: 829
Formulation: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Synonyms: DHP; HJMD; PCAD
Purification: Affinity purification
Background: This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a six-cadherin 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 have been associated with congential hypotrichosis with juvenile macular dystrophy. [provided by RefSeq, Jul 2008]
Storage: Store at 4℃. Avoid freeze / thaw cycles.
Recommended Dilutions: WB 1:500 - 1:2000, IHC 1:50 - 1:100, FC 1:20 - 1:50

Target (Information from UniProt)
Function: Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types.
Tissue Specificity: Expressed in some normal epithelial tissues and in some carcinoma cell lines.
Involvement in Disease: Hypotrichosis congenital with juvenile macular dystrophy: A disorder characterized by congenital hypotrichosis, early hair loss, and severe degenerative changes of the retinal macula that culminate in blindness during the second to third decade of life.

Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome: A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. It is an autosomal recessive condition characterized by features of ectodermal dysplasia such as sparse eyebrows and scalp hair, and selective tooth agenesis associated with macular dystrophy and ectrodactyly.
Cellular Location: Cell membrane.

Western Blot - Anti-P-Cadherin Antibody from ABclonal (A0915) - Antibody Supply Service
Western blot analysis of extracts of A431 cells lines, using CDH3 antibody.

Product Code - A0915
Size Price Quantity
100µl £243
200µl £372

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