ADAMTS2 Polyclonal 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.

• Description:

  This is a ADAMTS2 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms:

  A disintegrin and metalloproteinase with thrombospondin motifs 2, A disintegrin like and metalloprotease (reprolysin type) with thrombospondin type 1 motif 2, ADAM metallopeptidase with thrombospondin type 1 motif 2, ADAM TS 2, ADAM TS2, ADAM-TS 2, ADAM-TS2, ADA

• Swiss Prot:

  O95450

• Accession Number:

  NP055059

• Reactivity:

  Human, Mouse

• Immunogen:

  Synthetic peptide of human ADAMTS2

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  IHC, ELISA

• Purification Method:

  Antigen affinity purification

• Assay Type:

  Antibody

• Concentration:

  1.32 mg/mL

• Dilution:

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

• Buffer:

  PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

• Storage Conditions:

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

• Host or Source:

  Rabbit

• Isotype:

  IgG