C7orf42 Antikörper (AA 231-314) (Alexa Fluor 680)

Produktnummer ABIN4998667

Produktdetails anti-C7orf42 Antikörper (Alexa Fluor 680)

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Bindungsspezifität: AA 231-314

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C7orf42 Antikörper ist konjugiert mit Alexa Fluor 680

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

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf42

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 C7orf42

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Andere Bezeichnung: C7orf42 (C7orf42 Produkte)

Synonyme: C7orf42 antikoerper, c7orf42 antikoerper, TMEM248 antikoerper, MGC79534 antikoerper, C25H7orf42 antikoerper, 0610007L01Rik antikoerper, A930023A16Rik antikoerper, AW557951 antikoerper, G430067H08Rik antikoerper, zgc:103561 antikoerper, transmembrane protein 248 antikoerper, transmembrane protein 248 L homeolog antikoerper, TMEM248 antikoerper, tmem248.L antikoerper, tmem248 antikoerper, Tmem248 antikoerper

Hintergrund:

Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.

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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.

Gen-ID: 55069