Human A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) Protein

221€ (10 µg)
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935106861
info@markelab.com
name
Human A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx065067
tested applications
WB, SDS-PAGE
Description
Recombinant A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) is a recombinant Human protein produced in a Prokaryotic expression system (E. coli).
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Proteins and Peptides |
Immunogen Target | A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) |
Host | E. coli |
Origin | Human |
Conjugation | Unconjugated |
Observed MW | Molecular Weight: Calculated MW: 14.0 kDa Concentration: Prior to lyophilization: 200 µg/ml Sequence Fragment: Thr854-Ser967 Tag: N-terminal His tag |
Purity | > 95% |
Size 1 | 10 µg |
Size 2 | 50 µg |
Size 3 | 100 µg |
Size 4 | 200 µg |
Size 5 | 500 µg |
Form | Lyophilized To keep the original salt concentration, we recommend reconstituting to the original concentration prior to lyophilization (see Concentration) in ddH2O. If a lower concentration is required, dilute in PBS, pH 7.4. If a higher concentration is required, the product can be reconstituted directly in PBS, pH 7.4, though please note that this will change the overall salt concentration. The stock concentration should be between 0.1-1.0 mg/ml. Do not vortex. |
Tested Applications | WB, SDS-PAGE |
Buffer | Prior to lyophilization: PBS, pH 7.4, containing 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose and Proclin-300. |
Availability | Shipped within 5-12 working days. |
Storage | Store at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q9UHI8 |
Alias | METH1, KIAA1346, C3-C5,Metalloprotease And Thrombospondin-1,ADAM-TS1,ADAMTS-1 |
Background | Protein ADAMTS1 |
Status | RUO |
Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
ADAMTS1 (ADAM metallopeptidase with thrombospondin type 1 motif 1) is a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS1 contains several distinct domains, including a signal peptide, a propeptide region, a metalloproteinase domain, a disintegrin-like domain, a thrombospondin type 1 (TSP1) motif, and a spacer region. ADAMTS1 is expressed in various tissues during development and in adulthood. It is found in tissues such as the heart, lungs, kidneys, blood vessels, and skeletal tissues. Its expression is often regulated in response to physiological cues and pathological conditions. ADAMTS1 plays a crucial role in ECM remodeling by cleaving ECM proteins such as aggrecan, versican, and brevican. These proteolytic activities are essential for tissue development, maintenance, and repair. ADAMTS1 is also involved in angiogenesis, It can promote or inhibit angiogenesis depending on the context and interacting partners. ADAMTS1 influences endothelial cell migration, proliferation, and tube formation during blood vessel development and remodeling.ADAMTS1 has been implicated in modulating inflammation and immune responses. It can regulate the activity of cytokines, chemokines, and growth factors, influencing immune cell recruitment, activation, and function. ADAMTS1 expression is dysregulated in various cancers, including breast cancer, ovarian cancer, and prostate cancer. Its roles in ECM remodeling, angiogenesis, and inflammation contribute to tumor progression, invasion, metastasis, and angiogenesis.Dysregulation of ADAMTS1 activity has been associated with musculoskeletal disorders such as osteoarthritis and intervertebral disc degeneration. In these conditions, ADAMTS1 contributes to the degradation of ECM components within cartilage and intervertebral discs, leading to tissue degeneration and joint dysfunction. ADAMTS1 expression levels correlate with cancer progression and poor prognosis in several types of cancer. It promotes tumor growth, invasion, and metastasis by facilitating ECM remodeling, angiogenesis, and inflammation within the tumor microenvironment.
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