DGCR6L Antikörper (AA 108-135)

Produktnummer ABIN656835

Produktdetails anti-DGCR6L Antikörper

Target: DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))

Bindungsspezifität: AA 108-135

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DGCR6L Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This DGCR6L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 108-135 amino acids from the Central region of human DGCR6L.

Klon: RB21366

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: DGCR6L Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Haltbarkeit: 6 months

Details zu DGCR6L

Target: DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))

Andere Bezeichnung: DGCR6L (DGCR6L Produkte)

Synonyme: DGCR6L antikoerper, DiGeorge syndrome critical region gene 6-like antikoerper, DiGeorge syndrome critical region gene 6 like antikoerper, DGCR6L antikoerper

Hintergrund: This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome.

Molekulargewicht: 24932

Gen-ID: 85359

NCBI Accession: NP_150282

UniProt: Q9BY27