LSMEM1 antibody (AA 31-100) (Cy3)

Catalog No. ABIN1702737

The Cy3-conjugated Rabbit Polyclonal anti-LSMEM1 antibody (ABIN1702737) specifically detects LSMEM1 in WB, IF (cc) and IF (p). The antibody is reactive with Human samples.

Quick Overview for LSMEM1 antibody (AA 31-100) (Cy3) (ABIN1702737)

Target: LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LSMEM1 antibody is conjugated to Cy3

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

Product Details anti-LSMEM1 Antibody (Cy3)

Binding Specificity: AA 31-100

Purpose: C7orf53 Polyclonal Antibody, Cy3 Conjugated

Predicted Reactivity: Human,Mouse,Rat,Dog

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf53

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000), 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, 0.02 % 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: -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 LSMEM1

Target: LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))

Alternative Name: C7orf53

Background:

Synonyms: C7orf53, CG053_HUMAN, Chromosome 7 open reading frame 53, Coiled-coil domain-containing transmembrane protein C7orf53.

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 C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.

Gene ID: 286006