C3orf24 antibody (Biotin)

Catalog No. ABIN1404871

Product Details anti-C3orf24 Antibody (Biotin)

Target: C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C3orf24 antibody is conjugated to Biotin

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf24

Isotype: IgG

Application Details

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

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 C3orf24

Target: C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))

Alternative Name: C3orf24 (C3orf24 Products)

Synonyms: C3orf24 antibody, RGD1565997 antibody, FANCD2 opposite strand L homeolog antibody, FANCD2 opposite strand antibody, fancd2os.L antibody, FANCD2OS antibody, fancd2os antibody, Fancd2os antibody

Background:

Synonyms: C3orf24, CC024_HUMAN, chromosome 3 open reading frame 24, HSD19, hypothetical protein LOC115795, MGC40179, Uncharacterized protein C3orf24.

Background: C3orf24, also known as MGC40179, is a 177 amino acid protein that is 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: 115795