SCP2D1 Antikörper (AA 101-156) (Alexa Fluor 594)

Produktnummer ABIN2810756

Produktdetails anti-SCP2D1 Antikörper

Target: SCP2D1 (SCP2 Sterol-Binding Domain Containing 1 (SCP2D1))

Bindungsspezifität: AA 101-156

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SCP2D1 Antikörper ist konjugiert mit Alexa Fluor 594

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

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf79

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.

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu SCP2D1

Target: SCP2D1 (SCP2 Sterol-Binding Domain Containing 1 (SCP2D1))

Andere Bezeichnung: C20orf79 (SCP2D1 Produkte)

Synonyme: C20orf79 antikoerper, HSD22 antikoerper, dJ1068E13.2 antikoerper, C13H20orf79 antikoerper, 1700010M22Rik antikoerper, SCP2 sterol binding domain containing 1 antikoerper, SCP2 sterol-binding domain containing 1 antikoerper, SCP2D1 antikoerper, Scp2d1 antikoerper

Hintergrund:

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 C20orf79 gene product has been provisionally designated C20orf79 pending further characterization.

Subcellular location: Cytoplasm

Synonyms: Chromosome 20 open reading frame 79, dJ1068E13.2, HSD22, Hypothetical protein LOC140856, MGC138229, OTTHUMP00000030367, Sterol carrier protein 2 like protein, Uncharacterized protein C20orf79.

Gen-ID: 140856