CCDC117 antibody (AA 148-250) (HRP)

Catalog No. ABIN887039

Product Details anti-CCDC117 Antibody (HRP)

Target: CCDC117 (Coiled-Coil Domain Containing 117 (CCDC117))

Binding Specificity: AA 148-250

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC117 antibody is conjugated to HRP

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

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC117

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 CCDC117

Target: CCDC117 (Coiled-Coil Domain Containing 117 (CCDC117))

Alternative Name: CCDC117 (CCDC117 Products)

Synonyms: dJ366L4.1 antibody, 1110004K02Rik antibody, 1700026O03Rik antibody, AU018638 antibody, AU042822 antibody, AV173073 antibody, BC018601 antibody, coiled-coil domain containing 117 antibody, CCDC117 antibody, Ccdc117 antibody

Background:

Synonyms: CC117_HUMAN, Ccdc117, Coiled-coil domain-containing protein 117.

Background: CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein Bcr-Abl, a potent cell proliferation activator found in several types of leukemias.

Gene ID: 150275