C5orf35 Antikörper (AA 1-100) (Biotin)

Produktnummer ABIN1700136

Produktdetails anti-C5orf35 Antikörper (Biotin)

Target: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Bindungsspezifität: AA 1-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C5orf35 Antikörper ist konjugiert mit Biotin

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

Homologie: Human,Dog

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C5orf35

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
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.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C for 12 months.

Haltbarkeit: 12 months

Details zu C5orf35

Target: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Andere Bezeichnung: C5orf35 (C5orf35 Produkte)

Synonyme: DKFZp468C1120 antikoerper, C5orf35 antikoerper, SET domain containing 9 antikoerper, SETD9 antikoerper, setd9 antikoerper

Hintergrund:

Synonyms: C5orf35 chromosome 5 open reading frame 35, Chromosome 5 open reading frame 35, Hypothetical protein LOC133383, MGC33648, Uncharacterized protein C5orf35, SET domain-containing protein 9, SETD9_HUMAN.

Background: C5orf35 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.

Gen-ID: 133383