CCDC36 antibody (AA 172-472) (HRP)

Catalog No. ABIN7980913

The Rabbit Polyclonal anti-CCDC36 antibody is suitable to detect CCDC36 in samples from Human. It has been validated for WB, ELISA and IHC.

Quick Overview for CCDC36 antibody (AA 172-472) (HRP) (ABIN7980913)

Target: CCDC36 (Coiled-Coil Domain Containing 36 (CCDC36))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC36 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Product Details anti-CCDC36 Antibody (HRP)

Binding Specificity: AA 172-472

Purpose: Anti-CCDC36 Antibody HRP Conjugated

Specificity: No cross reactivity with other proteins.

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human CCDC36 recombinant protein (Position: E172-N472).

Isotype: IgG

Application Details

Application Notes: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for CCDC36

Target: CCDC36 (Coiled-Coil Domain Containing 36 (CCDC36))

Alternative Name: CCDC36

Background:

Background: CCDC36, also known as CT74 (cancer/testis antigen 74), is a 584 amino acid protein that contains coiled-coil domains and is expressed as three alternatively spliced isoforms. The gene encoding CCDC36 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene Full Name: interactor of HORMAD1 1

Gene ID: 339834

UniProt: Q8IYA8