Adamts2 antibody

Catalog No. ABIN7248080

Product Details anti-Adamts2 Antibody

Target: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Adamts2 antibody is un-conjugated

Application: Immunohistochemistry (IHC), ELISA

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Synthetic peptide of human ADAMTS2

Isotype: IgG

Application Details

Application Notes: IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.32 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Adamts2

Target: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Alternative Name: ADAMTS2 (Adamts2 Products)

Synonyms: ADAM-TS2 antibody, ADAMTS-2 antibody, ADAMTS-3 antibody, PCINP antibody, hPCPNI antibody, mKIAA4060 antibody, pNPI antibody, NPI antibody, PC I-NP antibody, PCI-NP antibody, PCPNI antibody, PNPI antibody, RGD1565950 antibody, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2 antibody, ADAM metallopeptidase with thrombospondin type 1 motif 2 antibody, ADAM metallopeptidase with thrombospondin type 1 motif, 2 antibody, Adamts2 antibody, ADAMTS2 antibody

Background: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) 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 enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants.

UniProt: O95450