Anti-MMP2 antibody [EPR1184] is a rabbit recombinant monoclonal antibody that is used to detect MMP2 in Flow cytometry (Intra), ICC/IF, Western blot. Suitable for Human, Mouse, Rat samples.
- Using biophysical QC, antibody identity is confirmed at a molecular level for unrivaled batch-batch consistency
- Cited in over 370 publications
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | IHC-P | ICC/IF | Flow Cyt (Intra) | |
---|---|---|---|---|
Human | Tested | Not recommended | Tested | Tested |
Mouse | Tested | Not recommended | Expected | Expected |
Rat | Tested | Not recommended | Expected | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/1000 - 1/5000 | Notes For Lysate preparation protocol, please refer to the protocol here. Compared with ab92536, Anti-MMP2 antibody [EPR17003-25] ab181286 has higher sensitivity. We recommend Anti-MMP2 antibody [EPR17003-25] ab181286 as an alternative for testing MMP2 in western blot. |
Species Rat | Dilution info 1/1000 - 1/5000 | Notes For Lysate preparation protocol, please refer to the protocol here. Compared with ab92536, Anti-MMP2 antibody [EPR17003-25] ab181286 has higher sensitivity. We recommend Anti-MMP2 antibody [EPR17003-25] ab181286 as an alternative for testing MMP2 in western blot. |
Species Human | Dilution info 1/1000 - 1/5000 | Notes For Lysate preparation protocol, please refer to the protocol here. Compared with ab92536, Anti-MMP2 antibody [EPR17003-25] ab181286 has higher sensitivity. We recommend Anti-MMP2 antibody [EPR17003-25] ab181286 as an alternative for testing MMP2 in western blot. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/250 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/400 | Notes For unpurified, use 1/70. ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
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Ubiquitinous metalloproteinase that is involved in diverse functions such as remodeling of the vasculature, angiogenesis, tissue repair, tumor invasion, inflammation, and atherosclerotic plaque rupture. As well as degrading extracellular matrix proteins, can also act on several nonmatrix proteins such as big endothelial 1 and beta-type CGRP promoting vasoconstriction. Also cleaves KISS at a Gly-|-Leu bond. Appears to have a role in myocardial cell death pathways. Contributes to myocardial oxidative stress by regulating the activity of GSK3beta. Cleaves GSK3beta in vitro. Involved in the formation of the fibrovascular tissues in association with MMP14. PEX, the C-terminal non-catalytic fragment of MMP2, possesses anti-angiogenic and anti-tumor properties and inhibits cell migration and cell adhesion to FGF2 and vitronectin. Ligand for integrinv/beta3 on the surface of blood vessels. Isoform 2. Mediates the proteolysis of CHUK/IKKA and initiates a primary innate immune response by inducing mitochondrial-nuclear stress signaling with activation of the pro-inflammatory NF-kappaB, NFAT and IRF transcriptional pathways.
CLG4A, MMP2, 72 kDa type IV collagenase, 72 kDa gelatinase, Gelatinase A, Matrix metalloproteinase-2, TBE-1, MMP-2
Anti-MMP2 antibody [EPR1184] is a rabbit recombinant monoclonal antibody that is used to detect MMP2 in Flow cytometry (Intra), ICC/IF, Western blot. Suitable for Human, Mouse, Rat samples.
- Using biophysical QC, antibody identity is confirmed at a molecular level for unrivaled batch-batch consistency
- Cited in over 370 publications
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
In Western Blot, this product typically gives a weaker signal in some hepatocarcinoma like HepG2, MHCC97L(PMID: 33184263 ) et al. Please use reconmended positive control when testing these cells.
Compared with ab92536, ab181286 has higher sensitivity. We recommend ab181286 as an alternative for testing MMP2 in western blot.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Blocking and diluting buffer and concentration: 5% NFDM /TBST.
Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 was used as GAPDH loading control.
Compared with ab92536, Anti-MMP2 antibody [EPR17003-25] ab181286 has higher sensitivity. We recommend Anti-MMP2 antibody [EPR17003-25] ab181286 as an alternative for testing MMP2 in western blot.
Lanes 1 - 5: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/1000 dilution
Lanes 1 - 5: Western blot - Anti-MMP2 antibody [EPR17003-25] (Anti-MMP2 antibody [EPR17003-25] ab181286)
Lane 1: HT-1080 (Human fibrosarcoma epithelial cell) whole cell lysate at 20 µg
Lane 2: Untreated HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3: HepG2 (Human hepatocellular carcinoma epithelial cell) treated with 300ng/ml BFA for 24 hours whole cell lysate at 20 µg
Lane 4: Huh7 (Human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 5: U-87 MG (Human glioblastoma-astrocytoma epithelial cell) whole cell lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 73 kDa
Exposure time: 60s
MMP2 Western blot staining using rabbit Anti-MMP2 antibody
The 72 KDa band is pro-MMP2 and the 69 KDa band is active-MMP2 reported by PMID 11489818 and 22190701.
This antibody shows low affinity in detecting mouse liver and HepG2 lysates which are positive for MMP2 reported by PMID 24096707 and 24297510.
All lanes: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/1000 dilution
Lane 1: L6 (Rat skeletal muscle myoblast) whole cell lysates prepared in 1%SDS Hot lysis method at 20 µg
Lane 2: Mouse liver lysates prepared in RIPA lysis method at 20 µg
Lane 3: Mouse liver lysates prepared in 1%SDS Hot lysis method at 20 µg
Lane 4: Raw264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysates prepared in RIPA lysis method at 20 µg
Lane 5: Raw264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysates prepared in 1%SDS Hot lysis method at 20 µg
Lane 6: HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysates prepared in RIPA lysis method at 20 µg
Lane 7: HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysates prepared in 1%SDS Hot lysis method at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 73 kDa
Observed band size: 69 kDa, 72 kDa
Exposure time: 10s
Blocking buffer: 5% NFDM/TBST
Dilution buffer: 5% NFDM/TBST
72kDa: propeptide; 64kDa: active form
All lanes: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/10000 dilution
Lane 1: L6 cell lysate at 20 µg
Lane 2: NIH/3T3 cell lysate at 20 µg
All lanes: HRP goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 73 kDa
Observed band size: 64 kDa, 72 kDa
Overlay histogram showing HeLa cells fixed in 4% PFA and stained with purified ab92536 at a dilution of 1 in 400 (red line). The secondary antibody used was FITC goat anti-rabbit at a dilution of 1 in 500. Rabbit monoclonal IgG was used as an isotype control (black line) and cells incubated in the absence of both primary and secondary antibody were used as a negative control (blue line).
All lanes: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/1000 dilution
Lane 1: L6 cell lysate at 10 µg
Lane 2: Fetal heart lysate at 10 µg
Lane 3: NIH/3T3 cell lysate at 10 µg
All lanes: HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size: 73 kDa
Immunofluorescence staining of PC-3 cells with purified ab92536 at a working dilution of 1/250, counter-stained with DAPI. The secondary antibody was Alexa Fluor® 488 goat anti-rabbit (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077), used at a dilution of 1/1000. Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291, a mouse anti-tubulin antibody (1/1000), was used to stain tubulin along with Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (Alexa Fluor® 594 goat anti-mouse, 1/1000), shown in the top right hand panel. The cells were fixed in 4% PFA and permeabilized using 0.1% Triton X 100. The negative controls are shown in bottom middle and right hand panels - for negative control 1, purified ab92536 was used at a dilution of 1/500 followed by an Alexa Fluor® 594 goat anti-mouse antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at a dilution of 1/500. For negative control 2, Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (mouse anti-tubulin) was used at a dilution of 1/500 followed by an Alexa Fluor® 488 goat anti-rabbit antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at a dilution of 1/400.
Blocking buffer: 5% NFDM/TBST
Dilution buffer: 5% NFDM/TBST
72kDa: propeptide; 64kDa: active form
All lanes: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/5000 dilution
All lanes: human skin at 10 µg
All lanes: HRP goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 73 kDa
Observed band size: 64 kDa, 72 kDa
Intracellular Flow Cytometry analysis of PC-3 (human prostate adenocarcinoma) cells labeling MMP2 with purified ab92536 at 1/180 dilution (10ug/ml) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. A Goat anti rabbit IgG (Alexa Fluorr® 488) (1/2000 dilution) was used as the secondary antibody. Rabbit monoclonal IgG (Black) was used as the isotype control, cells without incubation with primary antibody and secondary antibody (Blue) were used as the unlabeled control.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 was used as a GAPDH loading control.
Compared with ab92536, Anti-MMP2 antibody [EPR17003-25] ab181286 has higher sensitivity. We recommend Anti-MMP2 antibody [EPR17003-25] ab181286 as an alternative for testing MMP2 in western blot.
Lanes 1 - 3: Western blot - Anti-MMP2 antibody [EPR1184] (ab92536) at 1/1000 dilution
Lanes 1 - 3: Western blot - Anti-MMP2 antibody [EPR17003-25] (Anti-MMP2 antibody [EPR17003-25] ab181286)
Lane 1: Human plasma tissue lysate at 20 µg
Lane 2: Human brain tissue lysate at 20 µg
Lane 3: Human breast tissue lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 73 kDa
Observed band size: 69 kDa, 72 kDa
Exposure time: 60s
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