C7ORF57 antibody (AA 161-260) (FITC)

Catalog No. ABIN1710049

This Rabbit Polyclonal antibody specifically detects C7ORF57 in IF (cc) and IF (p). It exhibits reactivity toward Rat.

Quick Overview for C7ORF57 antibody (AA 161-260) (FITC) (ABIN1710049)

Target: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7ORF57 antibody is conjugated to FITC

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C7ORF57 Antibody (FITC)

Binding Specificity: AA 161-260

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf57

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C7ORF57

Target: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Alternative Name: C7orf57

Background:

Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.

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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.

Gene ID: 136288

UniProt: Q8NEG2