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SRP3118

Sigma-Aldrich

MMP-2 human

recombinant, expressed in E. coli, ≥98% (SDS-PAGE), ≥98% (HPLC), suitable for cell culture

Synonyme(s) :

Gelatinase A

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10 μG
343,00 €

343,00 €


Date d'expédition estimée le10 avril 2025


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10 μG
343,00 €

About This Item

Code UNSPSC :
12352204
Nomenclature NACRES :
NA.32

343,00 €


Date d'expédition estimée le10 avril 2025


Devis pour commande en gros

Source biologique

human

Produit recombinant

expressed in E. coli

Essai

≥98% (HPLC)
≥98% (SDS-PAGE)

Forme

lyophilized

Poids mol.

62.0 kDa

Conditionnement

pkg of 10 μg

Technique(s)

cell culture | mammalian: suitable

Impuretés

<0.1 EU/μg endotoxin, tested

Couleur

white to off-white

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Température de stockage

−20°C

Informations sur le gène

human ... MMP2(4313)

Description générale

Matrix metalloproteinases (MMPs) are a family of endoproteases that require zinc and calcium for expressing catalytic activity.[1] MMP-2 is a secreted collagenase with specificity toward Type IV, V, VII, and X collagens.[2] The gene is mapped to human chromosome 16q12.2.[3] Recombinant human MMP-2 is a 62kDa protein containing the entire catalytic N-terminal domain and the C-terminal domain (552 amino acids).

Actions biochimiques/physiologiques

Matrix metalloproteinases (MMPs) enzymes play a central role in the maintenance and remodeling of the extracellular matrix.[4] Elevated expression of their activity, caused either by up-regulation of their expression or down-regulation of their cognate inhibitors, which has been implicated in various degenerative disorders, including arthritis, cardiovascular disease, skeletal growth-plate disorders, and cancer metastasis.[5][6][7][8] High levels of MMP-2 are observed in the acute phase of transverse myelitis.[9] It is upregulated in colorectal carcinoma and is associated with poor survival outcome.[10] MMP-2 gene haplotypes are also linked with risk of thoracic aortic dissection, a cardiovascular disorder with high death rate.[11]

Séquence

MYNFFPRKPK WDKNQITYRI IGYTPDLDPE TVDDAFARAF QVWSDVTPLR FSRIHDGEAD IMINFGRWEH GDGYPFDGKD GLLAHAFAPG TGVGGDSHFD DDELWTLGEG QVVRVKYGNA DGEYCKFPFL FNGKEYNSCT DTGRSDGFLW CSTTYNFEKD GKYGFCPHEA LFTMGGNAEG QPCKFPFRFQ GTSYDSCTTE GRTDGYRWCG TTEDYDRDKK YGFCPETAMS TVGGNSEGAP CVFPFTFLGN KYESCTSAGR SDGKMWCATT ANYDDDRKWG FCPDQGYSLF LVAAHEFGHA MGLEHSQDPG ALMAPIYTYT KNFRLSQDDI KGIQELYGAS PDIDLGTGPT PTLGPVTPEI CKQDIVFDGI AQIRGEIFFF KDRFIWRTVT PRDKPMGPLL VATFWPELPE KIDAVYEAPQ EEKAVFFAGN EYWIYSASTL ERGYPKPLTS LGLPPDVQRV DAAFNWSKNK KTYIFAGDKF WRYNEVKKKM DPGFPKLIAD AWNAIPDNLD AVVDLQGGGH SYFFKGAYYL KLENQSLKSV KFGSIKSDWL GC

Forme physique

Lyophilized from 10 mM Sodium Phosphate, pH 7.5 + 0.1 mM Calcium Chloride.

Reconstitution

Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.5-1.0 mg/ml. Do not vortex. This solution can be stored at 2-8°C for up to 1 week. For extended storage, it is recommended to further dilute in a buffer containing a carrier protein (example 0.1% BSA) and store in working aliquots at -20°C to -80°C.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Anxun Wang et al.
BMC cancer, 8, 182-182 (2008-07-01)
Ameloblastomas are odontogenic neoplasms characterized by local invasiveness. This study was conducted to address the role of matrix metalloproteinase-2 (MMP-2) in the invasiveness of ameloblastomas. Plasmids containing either MMP-2 siRNA or tissue inhibitor of metalloproteinase-2 (TIMP-2) cDNA were created and
The association between inflammation-related genes and serum androgen levels in men: the prostate, lung, colorectal, and ovarian study.
Meyer TE
Prostate, 72, 65-71 (2012)
High expression of matrix metalloproteinases: MMP-2 and MMP-9 predicts poor survival outcome in colorectal carcinoma.
Salem N
Future Oncology, 12, 323-331 (2016)
Association of MMP-2 gene haplotypes with thoracic aortic dissection in chinese han population.
Liu O
BMC Cardiovascular Disorders, 16, doi: 10- doi: 10 (2016)
Takashi Temma et al.
PloS one, 9(7), e102180-e102180 (2014-07-11)
Since matrix metalloproteinase-2 (MMP-2) is an important marker of tumor malignancy, we developed an original drug design strategy, MMP-2 activity dependent anchoring probes (MDAP), for use in MMP-2 activity imaging, and evaluated the usefulness of this probe in in vitro

Questions

1–2 sur 2 questions  
  1. Can you confirm if this product is an activated form of MMP-2, or does it require activation with APMA?

    1 réponse
    1. The product SRP3118 does not need activation with APMA since it is not a pro-MMP; it is expressed as the mature sequence.

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  2. What is the test method for Product No. SRP3118-10UG, MMP-2 Recombinant Human?

    1 réponse
    1. The test method for Product No. SRP3118-10UG, MMP-2 Recombinant Human involves measuring the MMP-2 human bioactivity by its ability to cleave a chromogenic peptide MMP-2 substrate at room temperature. This was done at an MMP-2 concentration of 2.5 ug/ml, achieving 50% cleavage at an incubation time of approximately 25 minutes. The protocol specifies using a kit supplied by AnaSpec (Catolog#72095), which includes diluting the colorimetric substrate, reconstituting the MMP-2 sample with water, mixing the MMP-2 and substrate solution, and taking readings at 412nm every 10 minutes for about 90 minutes or until a steady reading is obtained.

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