DGCR6L antibody (AA 108-135)

Catalog No. ABIN656835

The Rabbit Polyclonal anti-DGCR6L antibody (Clone RB21366) (ABIN656835) specifically detects DGCR6L in WB. The antibody is reactive with Human samples.

Quick Overview for DGCR6L antibody (AA 108-135) (ABIN656835)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DGCR6L antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB21366

Product Details anti-DGCR6L Antibody

Binding Specificity: AA 108-135

Purification: 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.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

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

Storage: 4 °C,-20 °C

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

Expiry Date: 6 months

Target Details for DGCR6L

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

Alternative Name: DGCR6L

Background: 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.

Molecular Weight: 24932

Gene ID: 85359

NCBI Accession: NP_150282

UniProt: Q9BY27