C20orf141 antibody (Cy3)

Catalog No. ABIN1421975

The Rabbit Polyclonal anti-C20orf141 antibody has been validated for WB and IF (p). It is suitable to detect C20orf141 in samples from Human.

Quick Overview for C20orf141 antibody (Cy3) (ABIN1421975)

Target: C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf141 antibody is conjugated to Cy3

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C20orf141 Antibody (Cy3)

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20ORF141

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: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C20orf141

Target: C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

Alternative Name: C20ORF141

Background:

Synonyms: LOC128653, Chromosome 20 open reading frame 141, CT141_HUMAN.

Background: The gene encoding C20orf141 maps to human chromosome 20, which houses over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be 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. The C20orf141 gene product has been provisionally designated C20orf141 pending further characterization.

Gene ID: 128653