C21orf37 antibody (AA 1-50) (Cy5.5)

Catalog No. ABIN1705332

The Cy5.5-conjugated Rabbit Polyclonal anti-C21orf37 antibody (ABIN1705332) specifically detects C21orf37 in IF (cc) and IF (p). The antibody is reactive with Human samples.

Quick Overview for C21orf37 antibody (AA 1-50) (Cy5.5) (ABIN1705332)

Target: C21orf37 (C21ORF37) (Chromosome 21 Open Reading Frame 37 (C21ORF37))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C21orf37 antibody is conjugated to Cy5.5

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C21orf37 Antibody (Cy5.5)

Binding Specificity: AA 1-50

Purpose: C21orf37 Polyclonal Antibody, Cy5.5 Conjugated

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf37

Isotype: IgG

Application Details

Application Notes: IF(IHC-P)(1:50-200), IF(IHC-F)(1:50-200), IF(ICC)(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, 0.02 % 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 C21orf37

Target: C21orf37 (C21ORF37) (Chromosome 21 Open Reading Frame 37 (C21ORF37))

Alternative Name: C21orf37

Background:

Synonyms: Chromosome 21 open reading frame 37, hCG_1817258, Putative uncharacterized protein C21orf37, CU037_HUMAN.

Background: C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.