C7orf30 antibody (AA 101-200)

Catalog No. ABIN1714509

The Rabbit Polyclonal anti-C7orf30 antibody (ABIN1714509) specifically detects C7orf30 in WB, IF (cc), IF (p), IHC (fro) and IHC (p). The antibody is reactive with Human samples.

Quick Overview for C7orf30 antibody (AA 101-200) (ABIN1714509)

Target: C7orf30 (Chromosome 7 Open Reading Frame 30 (C7orf30))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7orf30 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-C7orf30 Antibody

Binding Specificity: AA 101-200

Purpose: C7orf30 Polyclonal Antibody

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf30

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for C7orf30

Target: C7orf30 (Chromosome 7 Open Reading Frame 30 (C7orf30))

Alternative Name: C7orf30

Background:

Synonyms: C7orf30, MASU1_HUMAN, Chromosome 7 open reading frame 30, Uncharacterized protein C7orf30.

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 C7orf30 gene product has been provisionally designated C7orf30 pending further characterization.

Gene ID: 115416