Western blot - MMP14/MT1-MMP Rabbit mAb (A0067)
Western blot analysis of various lysates using MMP14/MMP14/MT1-MMP Rabbit mAb (A0067) at 1:1000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 90s.
Western blot - MMP14/MT1-MMP Rabbit mAb (A0067)
Western blot analysis of various lysates using MMP14/MMP14/MT1-MMP Rabbit mAb (A0067) at 1:1000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 10s.
Immunohistochemistry - MMP14/MT1-MMP Rabbit mAb (A0067)
Immunohistochemistry analysis of paraffin-embedded Human liver tissue using MMP14/MT1-MMP Rabbit mAb (A0067) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
Immunohistochemistry - MMP14/MT1-MMP Rabbit mAb (A0067)
Immunohistochemistry analysis of paraffin-embedded Human spleen tissue using MMP14/MT1-MMP Rabbit mAb (A0067) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
Immunohistochemistry - MMP14/MT1-MMP Rabbit mAb (A0067)
Immunohistochemistry analysis of paraffin-embedded Mouse kidney tissue using MMP14/MT1-MMP Rabbit mAb (A0067) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
Flow CytoMetry - MMP14/MT1-MMP Rabbit mAb (A0067)
Flow cytometry: 1X10^6 MCF7 cells (negative control, left) and HT-1080 (right) cells were intracellularly-stained with MMP14/MT1-MMP Rabbit mAb (A0067, 2 μg/mL, orange line) or ABflo® 488 Rabbit IgG isotype control (AC042, 2 μg/mL, blue line), followed by Alexa Fluor® 488 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
Flow CytoMetry - MMP14/MT1-MMP Rabbit mAb (A0067)
Flow cytometry: 1X10^6 MCF7 cells (negative control, left) and HT-1080 (right) cells were intracellularly-stained with MMP14/MT1-MMP Rabbit mAb (A0067, 2 μg/mL, orange line) or ABflo® 488 Rabbit IgG isotype control (AC042, 2 μg/mL, blue line), followed by Alexa Fluor® 488 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
Flow CytoMetry - MMP14/MT1-MMP Rabbit mAb (A0067)
Flow cytometry: 1X10^6 MCF7 cells (negative control, left) and HT-1080 (right) cells were intracellularly-stained with MMP14/MT1-MMP Rabbit mAb (A0067, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (AC042, 2 μg/mL, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
Flow CytoMetry - MMP14/MT1-MMP Rabbit mAb (A0067)
Flow cytometry: 1X10^6 MCF7 cells (negative control, left) and HT-1080 (right) cells were intracellularly-stained with MMP14/MT1-MMP Rabbit mAb (A0067, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (AC042, 2 μg/mL, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).