ADAMTS10 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant ADAMTS10.
Immunogen
Recombinant protein corresponding to amino acids of human ADAMTS10.
Sequence
SLIVMVLARTELPALRYRFNAPIARDSLPPYSWHYAPWTKCSAQCAGGSQVQAVECRNQLDSSAVAPHYCSAHSKLPK
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:10-1:20)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. 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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human stomach with ADAMTS10 polyclonal antibody (Cat # PAB23637) shows strong cytoplasmic positivity in glandular cells at 1:10-1:20 dilution. -
Gene Info — ADAMTS10
Entrez GeneID
81794Protein Accession#
Q9H324Gene Name
ADAMTS10
Gene Alias
ADAM-TS10, WMS
Gene Description
ADAM metallopeptidase with thrombospondin type 1 motif, 10
Gene Ontology
HyperlinkGene Summary
This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq
Other Designations
Weill-Marchesani syndrome|a disintegrin and metalloproteinase with thrombospondin motifs 10|a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 10|a disintegrin-like and metalloprotease domain with thrombospondin typ
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