product summary
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company name :
HUABIO
product type :
antibody
product name :
MMP-2
catalog :
HA72$3308
quantity :
100μl
price :
385.00 USD
clonality :
monoclonal
host :
domestic rabbit
conjugate :
nonconjugated
clone name :
PSH11-26
reactivity :
human, mouse, rat
application :
western blot, immunoprecipitation, flow cytometry, immunohistochemistry - paraffin section
more info or order :
product information
SKU :
HA72$3308
Target name :
MMP-2
Species reactivity :
Human,Mouse,Rat
Applications :
WB,IF-Cell,IHC-P,FC,IP
Conjugate :
Non-conjugated
Immunogen :
Recombinant protein within human MMP-2 aa 1-660.
Uniprot id :
P08253>SwissProt: P08253 Human;SwissProt: P33434 Mouse;SwissProt: P33436 Rat
Host :
Rabbit
Clone number :
PSH11-26
Isotype :
IgG
Size :
100μl
List Price :
385.00 USD
Storage Buffer :
PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Form :
Liquid
Storage Instruction :
Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Purity :
Protein A affinity purified.
Product type :
Recombinant Rabbit monoclonal Antibody
Positive control :
U-87 MG cell lysate, NIH/3T3 cell lysate, L6 cell lysate, Mouse skin tissue lysate, Rat skin tissue lysate, U-87 MG, NIH/3T3, L6, human colon tissue, human placenta tissue, human skin tissue, mouse colon tissue, mouse skin tissue, rat colon tissue, rat placenta tissue, rat skin tissue.
Molecular wt :
Predicted band size: 74 kDa
Subcellular location :
Secreted, extracellular space, extracellular matrixm Membrane, Nucleus; Cytoplasm, Mitochondrion.
Concentration :
1 mg/mL.
Recommended dilutions :
WB: 1:2,000 ;IF-Cell: 1:100 ;IHC-P: 1:1,000 ;FC: 1:1,000 ;IP: 1-2μg/sample
Advanced Validation :
Relative expression (RE)
Pic img4 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_4.jpg
Pic legend4 :
Immunocytochemistry analysis of L6 cells labeling MMP-2 with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Pic img5 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_5.jpg
Pic legend5 :
Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img6 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_6.jpg
Pic legend6 :
Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img7 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_7.jpg
Pic legend7 :
Immunohistochemical analysis of paraffin-embedded human skin tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img8 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_8.jpg
Pic legend8 :
Immunohistochemical analysis of paraffin-embedded mouse colon tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img9 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_9.jpg
Pic legend9 :
Immunohistochemical analysis of paraffin-embedded mouse skin tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img10 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_10.jpg
Pic legend10 :
Immunohistochemical analysis of paraffin-embedded rat colon tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img11 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_11.jpg
Pic legend11 :
Immunohistochemical analysis of paraffin-embedded rat placenta tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img12 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_12.jpg
Pic legend12 :
Immunohistochemical analysis of paraffin-embedded rat skin tissue with Rabbit anti-MMP-2 antibody (HA72$3308) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA72$3308) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img13 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_13.jpg
Pic legend13 :
Flow cytometric analysis of HCT 116 (left, low expression) and U-87 MG (right, positive) cells labeling MMP-2. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA72$3308, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Pic img14 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_14.jpg
Pic legend14 :
Flow cytometric analysis of NIH/3T3 cells labeling MMP-2. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA72$3308, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Pic img15 :
https://storage.huabio.cn/huabio/productImg/HA72$3308_15.jpg
Pic legend15 :
MMP-2 was immunoprecipitated from 0.2 mg U-87 MG cell lysate with HA72$3308 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA72$3308 at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature. Lane 1: U-87 MG cell lysate (input) Lane 2: HA72$3308 IP in U-87 MG cell lysate Lane 3: Rabbit IgG instead of HA72$3308 in U-87 MG cell lysate Blocking/Dilution buffer: 5% NFDM/TBST Exposure time: 59 seconds; ECL: K1801
more info or order :
company information
HUABIO
Boston, Massachusetts
support@huabio.com
https://www.huabio.com
1-857-353-6600
headquarters: USA
Founded in 2007, HUABIO is dedicated to developing high-quality antibodies that advance innovation. We are passionate about the accuracy, efficiency, and consistency of our products. That is why we have invested in new production platforms, like recombinant rabbit monoclonals, alpaca nanobodies, and adopted aggressive QA standards to deliver cutting-edge antibodies with uncompromised quality.
We hope to see you at your next discovery!