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  • Featured Product
  • KD/KO Validated

MMP2 Monoclonal antibody, PBS Only

MMP2 Monoclonal Antibody for WB, IHC, Indirect ELISA

Host / Isotype

Mouse / IgG1

Reactivity

human, rat, mouse, pig

Applications

WB, IHC, Indirect ELISA

Conjugate

Unconjugated

CloneNo.

2B10D1

Cat no : 66366-1-PBS

Synonyms

72 kDa gelatinase, 72 kDa type IV collagenase, CLG4, CLG4A, Gelatinase A, Matrix metalloproteinase 2, MMP 2, MMP II, MMP2, MONA, TBE 1

Validation Data Gallery

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  • Western Blot (WB) analysis of various lysates using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis using 66366-1-Ig (same clone as 66366-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of U-251 cells using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of U-251 using 66366-1-Ig (same clone as 66366-1-PBS)

    WB result of MMP2 antibody (66366-1-Ig; 1:1000; incubated at room temperature for 1.5 hours) with sh-Control and sh-MMP2 transfected U-251 cells. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of human placenta tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of human placenta using 66366-1-Ig (same clone as 66366-1-PBS)

    human placenta tissue were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 Antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of pig heart tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of pig heart using 66366-1-Ig (same clone as 66366-1-PBS)

    pig heart tissue were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 Antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of rat heart tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of rat heart using 66366-1-Ig (same clone as 66366-1-PBS)

    rat heart tissue were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 Antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of human heart tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of human heart using 66366-1-Ig (same clone as 66366-1-PBS)

    human heart tissue were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 Antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of MCF-7 cells using MMP2 Monoclonal antibody (66366-1-Ig)

    WB analysis of MCF-7 using 66366-1-Ig (same clone as 66366-1-PBS)

    MCF-7 cells were subjected to SDS PAGE followed by western blot with 66366-1-Ig (MMP2 Antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Immunohistochemistry (IHC) staining of human breast cancer tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    IHC staining of human breast cancer using 66366-1-Ig (same clone as 66366-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue slide using 66366-1-Ig (MMP2 antibody) at dilution of 1:300 (under 10x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

  • Immunohistochemistry (IHC) staining of human breast cancer tissue using MMP2 Monoclonal antibody (66366-1-Ig)

    IHC staining of human breast cancer using 66366-1-Ig (same clone as 66366-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue slide using 66366-1-Ig (MMP2 antibody) at dilution of 1:300 (under 40x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66366-1-PBS in a different storage buffer formulation.

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Tested Applications

Recommended dilution

ApplicationDilution
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Published Applications

IHCSee 1 publications below

Product Information

66366-1-PBS targets MMP2 in WB, IHC, Indirect ELISA applications and shows reactivity with human, rat, mouse, pig samples.

Tested Reactivity human, rat, mouse, pig
Cited Reactivityhuman
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen MMP2 fusion protein Ag25039 相同性解析による交差性が予測される生物種
Full Name matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase)
Calculated molecular weight 72 kDa
Observed molecular weight 55-74 kDa
GenBank accession numberBC002576
Gene symbol MMP2
Gene ID (NCBI) 4313
RRIDAB_2881746
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

MMP2, also named as CLG4A, Gelatinase Am, TBE-1 and PEX, belongs to the peptidase M10A family. It is ubiquitinous metalloproteinase that is involved in diverse functions such as remodeling of the vasculature, angiogenesis, tissue repair, tumor invasion, inflammation, and atherosclerotic plaque rupture. MMP2 contributes to myocardial oxidative stress by regulating the activity of GSK3beta. It cleaves GSK3beta in vitro. MMP2 can be cleaved into PEX chain(~60kd).Western blot analysis showed that the 72 kDa and 62 kDa proteinase activities were pro-MMP2 and the active enzyme,respectively(PMID:11112697).

Publications

SpeciesApplicationTitle
humanIHC

Int J Mol Sci

Glial-Cell-Line-Derived Neurotrophic Factor Promotes Glioblastoma Cell Migration and Invasion via the SMAD2/3-SERPINE1-Signaling Axis

Authors - Xiaoxiao Guo
View Article