C10orf62 Antikörper (AbBy Fluor® 555)

Produktnummer ABIN1404557

Produktdetails anti-C10orf62 Antikörper (AbBy Fluor® 555)

Target: C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C10orf62 Antikörper ist konjugiert mit AbBy Fluor® 555

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C10orf62

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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 C10orf62

Target: C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

Andere Bezeichnung: C10orf62 (C10ORF62 Produkte)

Synonyme: bA548K23.1 antikoerper, chromosome 10 open reading frame 62 antikoerper, C10orf62 antikoerper

Hintergrund:

Synonyms: bA548K23.1, Hypothetical protein LOC414157, MERIT40, chromosome 10 open reading frame 62, NBA1, Uncharacterized protein C10orf62, CJ062_HUMAN .

Background: C10orf62 is a 223 amino acid protein encoded by a gene that maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Gen-ID: 414157