DGCR6L anticorps (AA 108-135)

N° du produit ABIN656835

Détail du produit anti-DGCR6L anticorps

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

Épitope: AA 108-135

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DGCR6L est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: 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.

Clone: RB21366

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: 4 °C,-20 °C

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

Date de péremption: 6 months

Détails sur DGCR6L

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

Autre désignation: DGCR6L (DGCR6L Produits)

Synonymes: anticorps DGCR6L, anticorps DiGeorge syndrome critical region gene 6-like, anticorps DiGeorge syndrome critical region gene 6 like, anticorps DGCR6L

Sujet: 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.

Poids moléculaire: 24932

ID gène: 85359

NCBI Accession: NP_150282

UniProt: Q9BY27