CCDC8 antibody (AA 165-270) (HRP)

Catalog No. ABIN888145

Product Details anti-CCDC8 Antibody (HRP)

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

Binding Specificity: AA 165-270

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC8 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

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: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 (CCDC8 Products)

Synonyms: 3M3 antibody, PPP1R20 antibody, p90 antibody, ENSMUSG00000041117 antibody, coiled-coil domain containing 8 antibody, CCDC8 antibody, Ccdc8 antibody

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