ADAMTSL2 antibody (AA 796-938)

Catalog No. ABIN1886666

The Rabbit Polyclonal anti-ADAMTSL2 antibody is suitable to detect ADAMTSL2 in samples from Human. It has been validated for WB.

Quick Overview for ADAMTSL2 antibody (AA 796-938) (ABIN1886666)

Target: ADAMTSL2 (ADAMTS-Like 2 (ADAMTSL2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ADAMTSL2 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-ADAMTSL2 Antibody

Binding Specificity: AA 796-938

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 796 and 938 of Human ADAMTSL2

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for ADAMTSL2

Target: ADAMTSL2 (ADAMTS-Like 2 (ADAMTSL2))

Alternative Name: ADAMTSL-2

Background: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like protein family.Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif.Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains.The protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily.It is a secreted glycoprotein that binds the cell surface and extracellular matrix, it also interacts with latent transforming growth factor beta binding protein 1.Mutations in this gene have been associated with geleophysic dysplasia.[provided by RefSeq]

Molecular Weight: 105 kDa

Gene ID: 9719

NCBI Accession: NP_055509, NM_014694