Mouse A Disintegrin And Metalloproteinase With Thrombospondin 12 (ADAMTS12) Protein

Este producto es parte de ADAMTS12 - ADAM metallopeptidase with thrombospondin type 1 motif 12
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234€ (10 µg)

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935106861
info@markelab.com
name
Mouse A Disintegrin And Metalloproteinase With Thrombospondin 12 (ADAMTS12) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx065072
tested applications
WB, SDS-PAGE

Description

Recombinant A Disintegrin And Metalloproteinase With Thrombospondin 12 (ADAMTS12) is a recombinant Mouse protein produced in a Prokaryotic expression system (E. coli).

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
A Disintegrin And Metalloproteinase With Thrombospondin 12 (ADAMTS12)
Host
E. coli
Origin
Mouse
Conjugation
Unconjugated
Observed MW
Molecular Weight: Calculated MW: 21.0 kDa
Concentration: Prior to lyophilization: 200 µg/ml
Sequence Fragment: Lys827-Pro1001
Tag: N-terminal His tag
Expression
Recombinant
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
Q8WZ42
Alias
Type 1 Motif 12,PRO4389,A Disintegrin And Metalloproteinase With Thrombospondin Motifs 12,ADAMTS-12,ADAM-TS12
Background
Protein ADAMTS12
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

ADAMTS12 (ADAM metallopeptidase with thrombospondin type 1 motif 12) is a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS12 contains several domains typical of the ADAMTS family, including a signal peptide, a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and multiple thrombospondin type 1 (TSP1) motifs. ADAMTS12 is expressed in various tissues during development and in adulthood. It is found in tissues such as the heart, lungs, kidneys, and skeletal tissues. ADAMTS12 plays a significant role in ECM remodeling by cleaving ECM proteins such as aggrecan, versican, and brevican ADAMTS12 is implicated in various aspects of tissue development, particularly in skeletal development. It is involved in processes such as chondrogenesis and osteogenesis , where it regulates ECM composition and structure. ADAMTS12 has been associated with inflammation and immune responses. It can regulate the activity of cytokines, chemokines, and growth factors, influencing immune cell recruitment, activation, and function. ADAMTS12 expression or activity may contribute to inflammatory disorders. ADAMTS12 expression levels have been found to be dysregulated in various cancers, including breast cancer, ovarian cancer, and colorectal cancer. Its roles in ECM remodeling and tissue development suggest potential contributions to tumor progression, invasion, and metastasis.Dysregulation of ADAMTS12 activity has been associated with musculoskeletal disorders such as osteoarthritis and intervertebral disc degeneration. In these conditions, ADAMTS12 contributes to the degradation of ECM components within cartilage and intervertebral discs, leading to tissue degeneration and joint dysfunction. ADAMTS12 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 and inflammation within the tumor microenvironment.

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