ADAMTS2 polyclonal antibody
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More Files
- More Functions
Western Blot (Tissue lysate)
Western blot analysis of human skin lysate with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 100 dilution.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of formalin-fixed paraffin-embedded human skin tissue with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 200 dilution.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of ADAMTS2.
Immunogen
A synthetic peptide corresponding to 16 amino acids at C-terminus of human ADAMTS2.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Peptide affinity purification
Recommend Usage
ELISA (1:1000-1:10000)
Western Blot (1:200-1:1000)
Immunohistochemistry (1:100-1:500)
The optimal working dilution should be determined by the end user.Storage Buffer
In buffer containing 0.02% sodium azide
Storage Instruction
Store at 4°C for three months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
Western blot analysis of human skin lysate with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 100 dilution.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of formalin-fixed paraffin-embedded human skin tissue with ADAMTS2 polyclonal antibody (Cat # PAB18817) at 1 : 200 dilution.Enzyme-linked Immunoabsorbent Assay
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Gene Info — ADAMTS2
Entrez GeneID
9509Gene Name
ADAMTS2
Gene Alias
ADAM-TS2, ADAMTS-3, NPI, PCINP, PCPNI, hPCPNI
Gene Description
ADAM metallopeptidase with thrombospondin type 1 motif, 2
Gene Ontology
HyperlinkGene Summary
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 two transcript variants. The short transcript encodes a protein which has no significant procollagen N-peptidase activity. [provided by RefSeq
Other Designations
a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2|procollagen I N-proteinase|procollagen N-endopeptidase
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