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Recombinant Mouse Mmp2 Protein, His-tagged

Cat.No. : Mmp2-1785M
Product Overview : Recombinant Mouse Mmp2 Protein (Tyr110-Cys662) with N-His tag was expressed in E. coli.
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Description : This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme that hydrolyzes collagens, gelatins, laminin, fibronectin and elastin. Mice lacking the encoded protein exhibit suppressed angiogenesis and attenuated features of human multicentric osteolysis with arthritis including abnormal skeletal and craniofacial development.
Source : E. coli
Species : Mouse
Tag : His
Form : Freeze-dried powder
Molecular Mass : Predicted Molecular Mass: 63.4 kDa
Accurate Molecular Mass: 63 kDa
Protein length : Tyr110-Cys662
Purity : > 97%
Applications : Positive Control; Immunogen; SDS-PAGE; WB.
Stability : The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 centigrade for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
Storage : Avoid repeated freeze/thaw cycles. Store at 2-8 centigrade for one month. Aliquot and store at -80 centigrade for 12 months.
Storage Buffer : PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
Reconstitution : Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.
Gene Name : Mmp2 matrix metallopeptidase 2 [ Mus musculus (house mouse) ]
Official Symbol : Mmp2
Synonyms : MMP2; matrix metallopeptidase 2; 72 kDa type IV collagenase; gelatinase A; 72kD gelatinase; 72kDa gelatinase; 72 kDa gelatinase; 72kD type IV collagenase; 72kDa type IV collagenase; matrix metalloproteinase 2; matrix metalloproteinase-2; GelA; Clg4a; MMP-2;
Gene ID : 17390
mRNA Refseq : NM_008610
Protein Refseq : NP_032636
UniProt ID : P33434

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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06/19/2021

    The solubility and ion exchange ability are very good, which is convenient for subsequent experimental treatment and purification.

    05/13/2021

      Kinetic parameters such as enzymatic reaction rate and binding affinity were tested in the early stage, and it was found that the protein performed well.

      03/16/2021

        MMP2 products undergo strict quality control to ensure the consistency and stability of each batch.

        Q&As (6)

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        How to regulate the activity of MMP2 in tumor therapy? 10/20/2022

        The activity of MMP2 is regulated by inhibitors and antibodies against it to inhibit tumor metastasis and invasion.

        How is MMP2 related to metastases that promote disease progression? 05/04/2022

        MMP2 interacts with some transfer factors, such as VEGF and EGF, to promote tumor metastasis and invasion.

        What are the application prospects of MMP2 inhibitors? 02/20/2022

        Inhibitors of MMP2 can be used as potential drug targets for the treatment of tumors, cardiovascular diseases and other related diseases.

        Does MMP2 interact with the tumor microenvironment? 09/15/2021

        MMP2 interacts with tumor cells, immune cells, blood vessels, etc. in the tumor microenvironment to affect tumor progression and treatment effect.

        What is the role of MMP2 in embryonic development? 10/18/2020

        It is involved in important processes such as morphogenesis, organ development and intraembryonic lymphatic vessel formation during embryonic development.

        What are the effects of MMP2 mutations in human disease? 10/13/2020

        Mutations in MMP2 may affect its protein structure and function, leading to the occurrence and progression of related diseases.

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