DRICH1/C22orf43 antibody (AA 1-100) (HRP)

Catalog No. ABIN1710918

Product Details anti-DRICH1/C22orf43 Antibody (HRP)

Target: DRICH1/C22orf43 (C22orf43) (Chromosome 22 Open Reading Frame 43 (C22orf43))

Binding Specificity: AA 1-100

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DRICH1/C22orf43 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Cross-Reactivity: Human, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C22orf43

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 DRICH1/C22orf43

Target: DRICH1/C22orf43 (C22orf43) (Chromosome 22 Open Reading Frame 43 (C22orf43))

Alternative Name: C22orf43 (C22orf43 Products)

Synonyms: aspartate rich 1 antibody, DRICH1 antibody

Background:

Synonyms: C22orf43, Chromosome 22 open reading frame 43, CV043_HUMAN, Putative uncharacterized protein C22orf43, Uncharacterized protein C22orf43.

Background: C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 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.

Gene ID: 51233