Description
Antibody Name: | ADAMTS17 Antibody |
Antibody SKU: | PACO03573 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | ELISA, IHC |
Recommended Dilutions: | IHC:1:100-1:300 |
Species Reactivity: | Human, Mouse |
Immunogen: | synthesized peptide derived from the Internal region of human ADAMTS-17. |
Form: | Liquid |
Storage Buffer: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Purification Method: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Synonyms: | ADAMTS17; A disintegrin and metalloproteinase with thrombospondin motifs 17; ADAM-TS 17; ADAM-TS17; ADAMTS-17 |
UniProt Protein Function: | ADAMTS17: Defects in ADAMTS17 are the cause of Weill-Marchesani- like syndrome (WMLS). It is a disorder characterized by many of the key features of Weill-Marchesani syndrome, including lenticular myopia, ectopia lentis, glaucoma, spherophakia and short stature. However, the characteristic brachydactyly or decreased joint flexibility of Weill-Marchesani syndrome are absent. 2 isoforms of the human protein are produced by alternative splicing.Protein type: EC 3.4.24.-; Secreted; Secreted, signal peptide; Protease; Motility/polarity/chemotaxisChromosomal Location of Human Ortholog: 15q24Disease: Weill-marchesani-like Syndrome |
UniProt Protein Details: | |
NCBI Summary: | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members 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 encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016] |
UniProt Code: | Q8TE56 |
NCBI GenInfo Identifier: | 296434401 |
NCBI Gene ID: | 170691 |
NCBI Accession: | Q8TE56.2 |
UniProt Secondary Accession: | Q8TE56,Q2I7G4, Q6ZN75 |
UniProt Related Accession: | Q8TE56 |
Molecular Weight: | 54,757 Da |
NCBI Full Name: | A disintegrin and metalloproteinase with thrombospondin motifs 17 |
NCBI Synonym Full Names: | ADAM metallopeptidase with thrombospondin type 1 motif 17 |
NCBI Official Symbol: | ADAMTS17 |
NCBI Official Synonym Symbols: | |
NCBI Protein Information: | A disintegrin and metalloproteinase with thrombospondin motifs 17 |
UniProt Protein Name: | A disintegrin and metalloproteinase with thrombospondin motifs 17 |
UniProt Synonym Protein Names: | |
Protein Family: | A disintegrin and metalloproteinase with thrombospondin motifs |
UniProt Gene Name: | ADAMTS17 |
UniProt Entry Name: | ATS17_HUMAN |