CCDC8 antibody (AA 165-270) (AbBy Fluor® 488)

Catalog No. ABIN888151

This Rabbit Polyclonal antibody specifically detects CCDC8 in WB, IF (cc) and IF (p). It exhibits reactivity toward Human and Mouse.

Quick Overview for CCDC8 antibody (AA 165-270) (AbBy Fluor® 488) (ABIN888151)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC8 antibody is conjugated to AbBy Fluor® 488

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CCDC8 Antibody (AbBy Fluor® 488)

Binding Specificity: AA 165-270

Cross-Reactivity: Human, Mouse

Predicted Reactivity: Rat,Dog,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC8

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for CCDC8

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

Alternative Name: CCDC8

Background:

Synonyms: CCDC8, CCDC8_HUMAN, Coiled-coil domain-containing protein 8, DKFZp564K0322, ENSMUSG00000041117, MGC72567.

Background: This gene 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 this gene are a cause of 3M syndrome-3 (3M3). [provided by RefSeq, Dec 2011].

Gene ID: 83987