RBBP8NL Antikörper (AA 21-120) (FITC)

Produktnummer ABIN1709997

Produktdetails anti-RBBP8NL Antikörper (FITC)

Target: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Bindungsspezifität: AA 21-120

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RBBP8NL Antikörper ist konjugiert mit FITC

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

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf151

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 RBBP8NL

Target: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Andere Bezeichnung: C20orf151 (RBBP8NL Produkte)

Synonyme: C20H20orf151 antikoerper, C20orf151 antikoerper, chromosome 20 C20orf151 homolog antikoerper, RBBP8 N-terminal like antikoerper, C20H20orf151 antikoerper, RBBP8NL antikoerper

Hintergrund:

Synonyms: C20orf151, Chromosome 20 open reading frame 151, CT151_HUMAN, RP5-908M14.6, Uncharacterized protein C20orf151.

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

Gen-ID: 140893