C20orf112 antibody (Alexa Fluor 555)

Catalog No. ABIN1404125

Product Details anti-C20orf112 Antibody (Alexa Fluor 555)

Target: C20orf112 (C20ORF112) (Chromosome 20 Open Reading Frame 112 (C20ORF112))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf112 antibody is conjugated to Alexa Fluor 555

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf112

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 C20orf112

Target: C20orf112 (C20ORF112) (Chromosome 20 Open Reading Frame 112 (C20ORF112))

Alternative Name: C20orf112 (C20ORF112 Products)

Synonyms: C20orf113 antibody, dJ1184F4.2 antibody, dJ1184F4.4 antibody, nucleolar protein 4 like antibody, NOL4L antibody

Background:

Synonyms: C20orf112, C20orf113, Chromosome 20 open reading frame 112, CT112_HUMAN, Hypothetical protein LOC140688, Uncharacterized protein C20orf112.

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 C20orf112 gene product has been provisionally designated C20orf112 pending further characterization.

Gene ID: 140688