C22orf26 antibody (AA 51-138) (FITC)

Catalog No. ABIN1709104

This Rabbit Polyclonal antibody specifically detects C22orf26 in WB, IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for C22orf26 antibody (AA 51-138) (FITC) (ABIN1709104)

Target: C22orf26 (C22ORF26) (Chromosome 22 Open Reading Frame 26 (C22ORF26))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C22orf26 antibody is conjugated to FITC

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

Product Details anti-C22orf26 Antibody (FITC)

Binding Specificity: AA 51-138

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C22orf26

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, 0.03 % 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 C22orf26

Target: C22orf26 (C22ORF26) (Chromosome 22 Open Reading Frame 26 (C22ORF26))

Alternative Name: C22orf26

Background:

Synonyms: C22orf26, Chromosome 22 open reading frame 26, CV026_HUMAN, FLJ10945, Putative uncharacterized protein C22orf26.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. 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. Translo-acations 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. The C22orf26 gene product has been provisionally designated C22orf26 pending further characterization.

Gene ID: 55267