LSMEM1 Antikörper (AA 31-100)

Produktnummer ABIN1714427

Der Kaninchen Polyklonal anti-LSMEM1 Antikörper wird verwendet zum Nachweis von LSMEM1 in Proben von Human. Er wurde validiert für ELISA, WB, IF (cc), IF (p), IHC (fro), IHC (p) und ICC.

Kurzübersicht für LSMEM1 Antikörper (AA 31-100) (ABIN1714427)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LSMEM1 Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Produktdetails anti-LSMEM1 Antikörper

Bindungsspezifität: AA 31-100

Homologie: Human,Mouse,Rat,Dog

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf53

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu LSMEM1

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

Andere Bezeichnung: C7orf53

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