GeneBio Systems
Recombinant Human MMP-2 Protein(Halo Tag)
Recombinant Human MMP-2 Protein(Halo Tag)
SKU:PDMH100466
Couldn't load pickup availability
Size:100μg
Storage:Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping:This product is provided as lyophilized powder which is shipped with ice packs.
Exp date:12 months
Category ID_II:Recombinant Proteins
Category ID_III:Others
Abbreviation:MMP-2
Target Synonym:Gelatinase A;72 kDa type IV collagenase;Matrix metalloproteinase-2;TBE-1
Research Areas:Cancer;Cardiovascular;Cell Biology;Developmental Biology
Conjugation:
Target Species:Human
Expression Host:Mammalian
Application:
Fusion tag:C-Halo
UNIProt ID:P08253
Accession:P08253
Background:Matrix Metalloproteinase-2 (MMP-2) is an enzyme that degrades components of the extracellular matrix and thus plays a pivotal role in cell migration during physiological and pathological processes. MMP-2 expression is dependent on extracellular matrix metalloproteinase inducer (EMMPRIN); Her2/neu; growth factors; cytokines; and hormones. Pro-MMP-2 activation needs MT1-MMP and TIMP-2 contribution. MMP-2 is changed in distribution and increased in amount in the ventral cochlear nucleus after unilateral cochlear ablation. A low level of MMP-2 is linked to favorable prognosis in patients with a hormone receptor-negative tumor; usually associated with high risk. As a zymogen requiring proteolytic activation for catalytic activity; MMP-2 has been implicated broadly in the invasion and metastasis of many cancer model systems; including human breast cancer (HBC). Blocking MMP-2 secretion and activation during breast carcinoma development may decrease metastasis. The detection of active MMP-2 alone or the rate of pro-MMP-2 and active MMP-2 is considered a very sensitive indicator of cancer metastasis. Modulation of MMP-2 expression and activation through specific inhibitors and activators may thus provide a new mechanism for breast cancer treatment.
Concentration:
Activity:Not validated for activity
Sequence:Ala30-Cys660
Purity:> 80% as determined by reducing SDS-PAGE.
Formulation:Lyophilized from a 0.2 μm filtered solution in PBS with 5% Trehalose and 5% Mannitol.
Reconstitution:It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis
Endotoxin:< 1.0 EU/mg of the protein as determined by the LAL method
Calculated MW:103.3 kDa
ObservedMW:100-110 kDa
