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ADAMTS-like protein

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Below are the list of possible ADAMTS-like protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

ADAMTS-like protein 1

 ADAMTS-like protein 1 ELISA Kit
 ADAMTS-like protein 1 Recombinant
 ADAMTS-like protein 1 Antibody
Also known as ADAMTS-like protein 1 (ADAMTSL-1) (Punctin-1).
ADAMTSL1: a secreted protein and member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) family. This protein lacks the metalloproteinase and disintegrin-like domains, which are typical of the ADAMTS family, but contains other ADAMTS domains, including the thrombospondin type 1 motif. This protein may have
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important functions in the extracellular matrix. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide
 Adamtsl1 ELISA Kit
 Adamtsl1 Recombinant
 Adamtsl1 Antibody
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ADAMTS-like protein 2

 ADAMTS-like protein 2 ELISA Kit
 ADAMTS-like protein 2 Recombinant
 ADAMTS-like protein 2 Antibody
Also known as ADAMTS-like protein 2 (ADAMTSL-2).
ADAMTSL2: Defects in ADAMTSL2 are the cause of geleophysic dysplasia type 1 (GPHYSD1). An autosomal recessive disorder characterized by severe short stature, short hands and feet, joint limitations, and skin thickening. Radiologic features include delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies. A
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ffected individuals have characteristic facial features including a 'happy' face with full cheeks, shortened nose, hypertelorism, long and flat philtrum, and thin upper lip. Other distinctive features include progressive cardiac valvular thickening often leading to an early death, toe walking, tracheal stenosis, respiratory insufficiency, and lysosomal-like storage vacuoles in various tissues.

Protein type: Extracellular matrix; Protease; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 9q34.2

Molecular Function: protein binding

Biological Process: negative regulation of transforming growth factor beta receptor signaling pathway

Disease: Geleophysic Dysplasia 1
 ADAMTSL2 ELISA Kit
 ADAMTSL2 Recombinant
 ADAMTSL2 Antibody
 KIAA0605 ELISA Kit
 KIAA0605 Recombinant
 KIAA0605 Antibody
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ADAMTS-like protein 3

 ADAMTS-like protein 3 ELISA Kit
 ADAMTS-like protein 3 Recombinant
 ADAMTS-like protein 3 Antibody
Also known as ADAMTS-like protein 3 (ADAMTSL-3) (Punctin-2).
ADAMTSL3: 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Protease; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 15q25.2

Molecular Function: protein binding
 ADAMTSL3 ELISA Kit
 ADAMTSL3 Recombinant
 ADAMTSL3 Antibody
 KIAA1233 ELISA Kit
 KIAA1233 Recombinant
 KIAA1233 Antibody
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ADAMTS-like protein 4

 ADAMTS-like protein 4 ELISA Kit
 ADAMTS-like protein 4 Recombinant
 ADAMTS-like protein 4 Antibody
Also known as ADAMTS-like protein 4 (ADAMTSL-4).
Positive regulation of apoptosis. May facilitate FBN1 microfibril biogenesis ().
 Adamtsl4 ELISA Kit
 Adamtsl4 Recombinant
 Adamtsl4 Antibody
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ADAMTS-like protein 5

 ADAMTS-like protein 5 ELISA Kit
 ADAMTS-like protein 5 Recombinant
 ADAMTS-like protein 5 Antibody
Also known as ADAMTS-like protein 5 (ADAMTSL-5) (Thrombospondin type-1 domain-containing protein 6).
ADAMTSL5: May play a role in modulation of fibrillin microfibrils in the extracellular matrix (ECM). Interacts with heparin, FBN1 and FBN2. 2 isoforms of the human protein are produced by alternative splicing

Protein type: Extracellular matrix; Protease; Secreted; Secreted, signal peptide
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Chromosomal Location of Human Ortholog: 19p13.3

Cellular Component: extracellular region; microfibril; proteinaceous extracellular matrix

Molecular Function: heparin binding
 ADAMTSL5 ELISA Kit
 ADAMTSL5 Recombinant
 ADAMTSL5 Antibody
 THSD6 ELISA Kit
 THSD6 Recombinant
 THSD6 Antibody
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