C3orf65 antibody (AA 1-100) (Biotin)

Catalog No. ABIN1699914

This anti-C3orf65 antibody is a Rabbit Polyclonal antibody detecting C3orf65 in WB, ELISA, IHC (fro) and IHC (p). Suitable for Human.

Quick Overview for C3orf65 antibody (AA 1-100) (Biotin) (ABIN1699914)

Target: C3orf65 (C3ORF65) (Chromosome 3 Open Reading Frame 65 (C3ORF65))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C3orf65 antibody is conjugated to Biotin

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

Product Details anti-C3orf65 Antibody (Biotin)

Binding Specificity: AA 1-100

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf65

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 C3orf65

Target: C3orf65 (C3ORF65) (Chromosome 3 Open Reading Frame 65 (C3ORF65))

Alternative Name: C3orf65

Background:

Synonyms: Chromosome 3 open reading frame 65, FLJ32900, CC065_HUMAN.

Background: C3orf65 (chromosome 3 open reading frame 65) is a 143 amino acid protein encoded by a gene that maps to human chromosome 3q27.2. 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.