FAM209B antibody (PE-Cy5.5)

Catalog No. ABIN1713070

This Rabbit Polyclonal antibody specifically detects FAM209B in WB. It exhibits reactivity toward Human.

Quick Overview for FAM209B antibody (PE-Cy5.5) (ABIN1713070)

Target: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM209B antibody is conjugated to PE-Cy5.5

Application: Western Blotting (WB)

Product Details anti-FAM209B Antibody (PE-Cy5.5)

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf107

Isotype: IgG

Application Details

Application Notes: FCM(1:100-500)
Optimal working dilution should be determined by the investigator.

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

Expiry Date: 12 months

Target Details for FAM209B

Target: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Alternative Name: C20orf107

Background:

Synonyms: C20orf107, Chromosome 20 open reading frame 107, CT107_HUMAN, dJ1153D9.4, Hypothetical protein LOC388799, MGC104273, Uncharacterized protein C20orf107.

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 C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

Gene ID: 388799