CCDC8 antibody

Catalog No. ABIN7227634

This anti-CCDC8 antibody is a Rabbit Polyclonal antibody detecting CCDC8 in WB and ELISA. Suitable for Human.

Quick Overview for CCDC8 antibody (ABIN7227634)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC8 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CCDC8 Antibody

Purpose: CCDC8 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of CCDC8 protein

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

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

Isotype: IgG

Application Details

Application Notes: 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).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

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: 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.

Target Details for CCDC8

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

Alternative Name: CCDC8

Background: 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

Molecular Weight: observerd band 59kDa

Gene ID: 83987

UniProt: Q9H0W5