C20orf194 antibody (FITC)

Catalog No. ABIN1404152

The Rabbit Polyclonal anti-C20orf194 antibody has been validated for WB. It is suitable to detect C20orf194 in samples from Human, Mouse and Rat.

Quick Overview for C20orf194 antibody (FITC) (ABIN1404152)

Target: C20orf194 (Chromosome 20 Open Reading Frame 194 (C20orf194))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf194 antibody is conjugated to FITC

Application: Western Blotting (WB)

Product Details anti-C20orf194 Antibody (FITC)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf194

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 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: 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 C20orf194

Target: C20orf194 (Chromosome 20 Open Reading Frame 194 (C20orf194))

Alternative Name: C20orf194

Background:

Synonyms: chromosome 20 open reading frame 194, DKFZp434N061, hypothetical protein LOC25943, MGC117480, MGC141683, Uncharacterized protein C20orf194, CT194_HUMAN .

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 C20orf194 gene product has been provisionally designated C20orf194 pending further characterization.

Gene ID: 25943

UniProt: Q5TEA3