C7orf45 Antikörper (AA 51-150) (HRP)

Produktnummer ABIN1711173

Produktdetails anti-C7orf45 Antikörper (HRP)

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

Bindungsspezifität: AA 51-150

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C7orf45 Antikörper ist konjugiert mit HRP

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

Homologie: Human,Mouse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf45

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC-P 1:200-400
IHC-F 1:100-500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu C7orf45

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

Andere Bezeichnung: C7orf45 (SSMEM1 Produkte)

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

Hintergrund:

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.

Gen-ID: 136263