C7orf64 antibody (AA 1-100)

Catalog No. ABIN1714045

This Rabbit Polyclonal antibody specifically detects C7orf64 in WB, IF (cc), IF (p), IHC (fro) and IHC (p). It exhibits reactivity toward Human.

Quick Overview for C7orf64 antibody (AA 1-100) (ABIN1714045)

Target: C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7orf64 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-C7orf64 Antibody

Binding Specificity: AA 1-100

Purpose: C7orf64 Polyclonal Antibody

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf64

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 C7orf64

Target: C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))

Alternative Name: C7orf64

Background:

Synonyms: C7orf64, RBM48_HUMAN, DKFZP564O0523, DKFZp686D1651, HSPC304, Hypothetical protein LOC84060, OTTHUMP00000215752, UPF0712 protein C7orf64.

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 C7orf64 gene product has been provisionally designated C7orf64 pending further characterization.

Gene ID: 84060