LSMEM1 Antikörper (AA 31-100) (FITC)

Produktnummer ABIN1710128

Produktdetails anti-LSMEM1 Antikörper (FITC)

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

Bindungsspezifität: AA 31-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LSMEM1 Antikörper ist konjugiert mit FITC

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

Homologie: Human,Mouse,Rat,Dog

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf53

Isotyp: IgG

Anwendungsinformationen

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

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.

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 LSMEM1

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

Andere Bezeichnung: C7orf53 (C7ORF53 Produkte)

Synonyme: C7orf53 antikoerper, Gm889 antikoerper, C4H7orf53 antikoerper, C1H7orf53 antikoerper, C7ORF53 antikoerper, leucine rich single-pass membrane protein 1 antikoerper, leucine-rich single-pass membrane protein 1 antikoerper, LSMEM1 antikoerper, Lsmem1 antikoerper

Hintergrund:

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.

Gen-ID: 286006