CCDC8 anticorps

N° du produit ABIN7227634

Cet anticorps anti-CCDC8 est un anticorps Lapin Polyclonal détectant CCDC8 dans WB et ELISA. Adapté pour Humain.

Aperçu rapide pour CCDC8 anticorps (ABIN7227634)

Antigène: CCDC8 (Coiled-Coil Domain Containing 8 (CCDC8))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC8 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CCDC8 anticorps

Fonction: CCDC8 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CCDC8 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human CCDC8 protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur CCDC8

Antigène: CCDC8 (Coiled-Coil Domain Containing 8 (CCDC8))

Autre désignation: CCDC8

Sujet: Rabbit Anti-CCDC8 Polyclonal Antibody,Coiled-coil domain-containing protein 8,CCDC8 (Coiled-Coil Domain Containing 8) is a Protein Coding gene. Diseases associated with CCDC8 include 3-M Syndrome 3 and 3-M Syndrome, Ccdc8-Related. CCDC8 encodes a coiled-coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1. Mutations in CCDC8 are a cause of 3M syndrome-3 (3M3).,CCDC8

Poids moléculaire: observerd band 59kDa

ID gène: 83987

UniProt: Q9H0W5