ADAMTSL2 anticorps (AA 796-938)

N° du produit ABIN1886666

L’anticorps anti-ADAMTSL2 Polyclonal Lapin est utilisé pour la détection de ADAMTSL2 dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour ADAMTSL2 anticorps (AA 796-938) (ABIN1886666)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ADAMTSL2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ADAMTSL2 anticorps

Épitope: AA 796-938

Purification: Purified by antigen-affinity chromatography.

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

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

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

Détails sur ADAMTSL2

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

Autre désignation: ADAMTSL-2

Sujet: 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]

Poids moléculaire: 105 kDa

ID gène: 9719

NCBI Accession: NP_055509, NM_014694