MMP2 (NM_004530) Human Untagged Clone
SKU
SC321560
MMP2 (untagged)-Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1
$923.00
In Stock*
Specifications
| Product Data | |
| Type | Human Untagged Clone |
|---|---|
| Target Symbol | MMP2 |
| Synonyms | CLG4; CLG4A; MMP-2; MMP-II; MONA; TBE-1 |
| Vector | pCMV6-AC |
| E. coli Selection | Ampicillin (100 ug/mL) |
| Mammalian Cell Selection | Neomycin |
| Sequence Data | |
| Restriction Sites | Please inquire | |
| ACCN | NM_004530 |
| OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA. |
| Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
| Reconstitution Method | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
| Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
| Shipping | Ambient |
| Reference Data | |
| RefSeq | NM_004530.1, NP_004521.1 |
| RefSeq Size | 3069 bp |
| RefSeq ORF | 1983 bp |
| Locus ID | 4313 |
| UniProt ID | P08253 |
| Cytogenetics | 16q12.2 |
| Domains | FN2, hemopexin, Peptidase_M10, ZnMc |
| Protein Families | Druggable Genome, Protease |
| Protein Pathways | Bladder cancer, GnRH signaling pathway, Leukocyte transendothelial migration, Pathways in cancer |
| Summary | This gene is a member of the matrix metalloproteinase (MMP) gene family, that are zinc-dependent enzymes capable of cleaving components of the extracellular matrix and molecules involved in signal transduction. The protein encoded by this gene is a gelatinase A, type IV collagenase, that contains three fibronectin type II repeats in its catalytic site that allow binding of denatured type IV and V collagen and elastin. Unlike most MMP family members, activation of this protein can occur on the cell membrane. This enzyme can be activated extracellularly by proteases, or, intracellulary by its S-glutathiolation with no requirement for proteolytical removal of the pro-domain. This protein is thought to be involved in multiple pathways including roles in the nervous system, endometrial menstrual breakdown, regulation of vascularization, and metastasis. Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. provided by RefSeq, Oct 2014 Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). |
Reviews
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
"NM_004530" in other vectors (6)
| SKU | Description | Size | Price | |
|---|---|---|---|---|
| RC200720 | MMP2 (Myc-DDK-tagged)-Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1 | 10 ug |
$921.00
|
|
| RC200720L1 | Lenti ORF clone of Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1, Myc-DDK-tagged | 10 ug |
$1,221.00
|
|
| RC200720L2 | Lenti ORF clone of Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1, mGFP tagged | 10 ug |
$1,221.00
|
|
| RC200720L3 | Lenti ORF clone of Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1, Myc-DDK-tagged | 10 ug |
$1,221.00
|
|
| RC200720L4 | Lenti ORF clone of Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1, mGFP tagged | 10 ug |
$1,221.00
|
|
| RG200720 | MMP2 (tGFP-tagged) - Human matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (MMP2), transcript variant 1 | 10 ug |
$1,121.00
|
|
Citations
The cytoplasmic domain of MT1-MMP is dispensable for migration augmentation but necessary to mediate viability of MCF-7 breast cancer cells
Cepeda, Pelling, Evered et al
Exp. Cell Res. (2016)
Cepeda, Pelling, Evered et al
Exp. Cell Res. (2016)
Less is more: low expression of MT1-MMP is optimal to promote migration and tumourigenesis of breast cancer cells
Cepeda, Pelling, Evered et al
Mol. Cancer (2016) 15 (1), 65 DOI: 10.1186/s12943-016-0547-x
Cepeda, Pelling, Evered et al
Mol. Cancer (2016) 15 (1), 65 DOI: 10.1186/s12943-016-0547-x
AI Summary: OriGene contributed to this study by providing human MT1-MMP (sc116990), TIMP-2 (sc118083), and MMP-2 (sc321560) cDNA clones, which were used to investigate the effects of MT1-MMP expression on breast cancer cell migration and tumorigenesis.
Snippet: CO 2 . cDNA clones and reagents. Human MT1-MMP (sc116990), TIMP-2(sc118083) and MMP-2 (sc321560) cDNA clones were purchased from Origene andsubcloned into the vector pcDNA 3.3 (Thermo Fisher). The generation ... Cite SaveSaving
The Human Ether-a-go-go-Related Gene (hERG) Potassium Channel Represents an Unusual Target for Protease-mediated Damage
Lamothe, Guo, Li et al
J. Biol. Chem. (2016)
Lamothe, Guo, Li et al
J. Biol. Chem. (2016)
Expression profile of genes involved in pathogenesis of pediatric Crohn's disease
Sim, Wagner, Cameron et al
J. Gastroenterol. Hepatol. (2012) 27 (6), 1083-93 DOI: 10.1111/j.1440-1746.2011.06973.x
Sim, Wagner, Cameron et al
J. Gastroenterol. Hepatol. (2012) 27 (6), 1083-93 DOI: 10.1111/j.1440-1746.2011.06973.x
Cited by 19
Nanolitre liquid patterning in aqueous environments for spatially defined reagent delivery to mammalian cells
Tavana, Jovic, Mosadegh et al
Nat Mater (2009) 8 (9), 736-41 DOI: 10.1038/nmat2515
Tavana, Jovic, Mosadegh et al
Nat Mater (2009) 8 (9), 736-41 DOI: 10.1038/nmat2515
Cited by 239
AI Summary: In this paper, OriGene products—specifically, HuSH shRNA plasmids and TurboGFP cDNA—were used to demonstrate patterned delivery and expression of genetic materials in mammalian cells, validating the effectiveness of the nanolitre liquid patterning technique for spatially defined gene expression and silencing.
Identification of amino acid residues of matrix metalloproteinase-7 essential for binding to cholesterol sulfate
Higashi, Oeda, Yamamoto et al
J Biol Chem (2008) 283 (51), 35735-44 DOI: 10.1074/jbc.M806285200
Higashi, Oeda, Yamamoto et al
J Biol Chem (2008) 283 (51), 35735-44 DOI: 10.1074/jbc.M806285200
AI Summary: In this study, OriGene products—including the human MMP7 cDNA clone (OriGene, SC119210) and the human MMP2 cDNA clone (OriGene, SC127460)—were used to construct chimeric and mutant proteases, enabling the identification of specific amino acid residues in MMP-7 that are essential for binding to cholesterol sulfate.
Showing 1-6 of 7 papers.
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