CCDC36 antibody (AA 172-472)

Catalog No. ABIN7871265

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

Quick Overview for CCDC36 antibody (AA 172-472) (ABIN7871265)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC36 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-CCDC36 Antibody

Binding Specificity: AA 172-472

Purpose: CCDC36 Antibody

Purification: Antigen affinity purified

Immunogen: Amino acids E172-N472 from the human protein were used as the immunogen for the CCDC36 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the CCDC36 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the CCDC36 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for CCDC36

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

Alternative Name: CCDC36

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.

UniProt: Q8IYA8