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Invitrogen™ SSMEM1 Polyclonal Antibody
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Catalog No. FEPA5144166
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100 μg
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Catalog No. Quantity
FEPA5144166 100 μg
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Catalog No. FEPA5144166 Supplier Invitrogen™ Supplier No. PA5144166
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Description

Rabbit Polyclonal Antibody

SSMEM1 Polyclonal Antibody for ICC/IF, IHC (P), ELISA

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen SSMEM1
Applications ELISA, Immunohistochemistry (Paraffin), Immunocytochemistry
Classification Polyclonal
Concentration 5 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.03% Proclin 300; pH 7.4
Gene SSMEM1
Gene Accession No. Q8WWF3
Gene Alias 1700016K02Rik; 1700025E21Rik; C7orf45; serine rich single-pass membrane protein 1; serine-rich single-pass membrane protein 1; SSMEM1
Gene Symbols SSMEM1
Host Species Rabbit
Immunogen Recombinant Human Serine-rich single-pass membrane protein 1 protein (56-244AA).
Purification Method Protein G
Quantity 100 μg
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 136263
Target Species Human
Content And Storage -20°C or -80°C if preferred
Product Type Antibody
Form Liquid
Isotype IgG
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