C20orf166 antibody (AA 21-117) (Biotin)

Catalog No. ABIN1699890

Product Details anti-C20orf166 Antibody (Biotin)

Target: C20orf166 (Chromosome 20 Open Reading Frame 166 (C20orf166))

Binding Specificity: AA 21-117

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf166 antibody is conjugated to Biotin

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

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf166

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.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for C20orf166

Target: C20orf166 (Chromosome 20 Open Reading Frame 166 (C20orf166))

Alternative Name: C20orf166 (C20orf166 Products)

Synonyms: dJ353C17.1 antibody, MIR1-1 host gene antibody, MIR1-1HG antibody

Background:

Synonyms: C20orf166, Chromosome 20 open reading frame 166, CT166_HUMAN, dJ353C17.1, RP3-353C17.2, Uncharacterized protein C20orf166.

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf166 gene product has been provisionally designated C20orf166 pending further characterization.

Gene ID: 128826