CCDC102B antibody (AA 81-130)

Catalog No. ABIN1451172

The Rabbit Polyclonal anti-CCDC102B antibody (ABIN1451172) specifically detects CCDC102B in WB, IHC, ELISA and IF. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for CCDC102B antibody (AA 81-130) (ABIN1451172)

Target: CCDC102B (Coiled-Coil Domain Containing 102B (CCDC102B))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC102B antibody is un-conjugated

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

Product Details anti-CCDC102B Antibody

Binding Specificity: AA 81-130

Purpose: CCDC102B Antibody

Specificity: CCDC102B Polyclonal Antibody detects endogenous levels of CCDC102B protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: The antiserum was produced against synthesized peptide derived from human CCDC102B. AA range:81-130

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for CCDC102B

Target: CCDC102B (Coiled-Coil Domain Containing 102B (CCDC102B))

Alternative Name: CCDC102B

Background:

Synonyms: CCDC102B, C18orf14, Coiled-coil domain-containing protein 102B

Background: CCDC102B (coiled-coil domain containing 102B), also known as AN, ACY1L or HsT1731, is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV (copy-number variant) regions, CCDC102B contains the deletion breakpoint of a maternally inherited deletion, which is 2.7Mb in size, and maps to human chromosome 18q22.1. CCDC102B may play a role in the pathogenesis of diaphragmatic hernia, microphthalmia, colorectal carcinoma and schizophrenia. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Translocation between chromosomes 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18.

Gene Name: CCDC102B

Protein Name: Coiled-coil domain-containing protein 102B

Molecular Weight: 60 kDa

Gene ID: 79839

UniProt: Q68D86