C22orf25 antibody (AA 25-75) (Alexa Fluor 750)

Catalog No. ABIN4998330

Product Details anti-C22orf25 Antibody (Alexa Fluor 750)

Target: C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))

Binding Specificity: AA 25-75

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C22orf25 antibody is conjugated to Alexa Fluor 750

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 C22orf25

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 C22orf25

Target: C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))

Alternative Name: C22orf25 (C22orf25 Products)

Synonyms: c22orf25 antibody, MGC88919 antibody, C22orf25 antibody, TANGO2 antibody, C17H22orf25 antibody, transport and golgi organization 2 homolog L homeolog antibody, transport and golgi organization 2 homolog antibody, transport and golgi organization 2 homolog (Drosophila) antibody, tango2.L antibody, tango2 antibody, TANGO2 antibody

Background:

Synonyms: Uncharacterized protein C22orf25, chromosome 22 open reading frame 25, DKFZp 761 P 1121, Hypothetical protein LOC128989, TNG2_HUMAN, TANGO2, Transport and Golgi organization protein 2 homolog.

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. 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. The C22orf25 gene product has been provisionally designated C22orf25 pending further characterization.

Gene ID: 128989

UniProt: Q6ICL3