CCDC102B anticorps (AA 81-130)

N° du produit ABIN1451172

Cet anticorps anti-CCDC102B Polyclonal Lapin (ABIN1451172) détecte spécifiquement CCDC102B dans WB, IHC, ELISA et IF. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour CCDC102B anticorps (AA 81-130) (ABIN1451172)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC102B est non-conjugé

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

Détail du produit anti-CCDC102B anticorps

Épitope: AA 81-130

Fonction: CCDC102B Antibody

Specificité: 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.

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

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur CCDC102B

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

Autre désignation: CCDC102B

Sujet:

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

Poids moléculaire: 60 kDa

ID gène: 79839

UniProt: Q68D86