Chromosome 7 Open Reading Frame 10 (C7orf10) antibody (Biotin)

Catalog No. ABIN1701006

Product Details

Target: Chromosome 7 Open Reading Frame 10 (C7orf10)

See all Chromosome 7 Open Reading Frame 10 (C7orf10) Antibodies

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: Biotin

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf10

Isotype: IgG

Application Details

Application Notes: WB 1:100-1000
IHC-P 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C

Storage Comment: Store at 4°C

Expiry Date: 12 months

Target Details

Target: Chromosome 7 Open Reading Frame 10 (C7orf10)

See all Chromosome 7 Open Reading Frame 10 (C7orf10) Antibodies

Alternative Name: C7orf10 (C7orf10 Antibody Abstract)

Synonyms: DERP13, ORF19, c7orf10, sugct, succinyl-CoA:glutarate-CoA transferase, succinyl-CoA:glutarate-CoA transferase L homeolog, SUGCT, sugct.L

Background:

Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.

Synonyms: Chromosome 7 open reading frame 10, Dermal papilla derived protein 13, DERP13, FLJ11808, Hypothetical protein LOC79783, ORF19, Russel-Silver syndrome candidate, Uncharacterized protein C7orf10,CG010_HUMAN.

Gene ID: 79783