C3ORF36 antibody (AA 81-165) (Biotin)

Catalog No. ABIN1699912

Product Details anti-C3ORF36 Antibody (Biotin)

Target: C3ORF36 (Chromosome 3 Open Reading Frame 36 (C3ORF36))

Binding Specificity: AA 81-165

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C3ORF36 antibody is conjugated to Biotin

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

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf36

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.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for C3ORF36

Target: C3ORF36 (Chromosome 3 Open Reading Frame 36 (C3ORF36))

Alternative Name: C3orf36 (C3ORF36 Products)

Synonyms: chromosome 3 open reading frame 36 antibody, C3orf36 antibody

Background:

Synonyms: C3orf36, CC036_HUMAN, Chromosome 3 open reading frame 36, Uncharacterized protein C3orf36.

Background: C3orf36 (chromosome 3 open reading frame 36), also known as FLJ22173, MGC125760 or MGC125761, is a 165 amino acid protein encoded by a gene that maps to human chromosome 3p25.3. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene ID: 80111