C7orf45 antibody (AA 51-150) (HRP)

Catalog No. ABIN1711173

Product Details anti-C7orf45 Antibody (HRP)

Target: C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))

Binding Specificity: AA 51-150

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7orf45 antibody is conjugated to HRP

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Predicted Reactivity: Human,Mouse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf45

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 C7orf45

Target: C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))

Alternative Name: C7orf45 (SSMEM1 Products)

Synonyms: C7orf45 antibody, RGD1559502 antibody, 1700016K02Rik antibody, 1700025E21Rik antibody, serine rich single-pass membrane protein 1 antibody, serine-rich single-pass membrane protein 1 antibody, SSMEM1 antibody, Ssmem1 antibody

Background:

Synonyms: C7orf45, CG045_HUMAN, chromosome 7 open reading frame 45, FLJ40316, Uncharacterized protein C7orf45.

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 C7orf45 gene product has been provisionally designated C7orf45 pending further characterization.

Gene ID: 136263