Anti-PKM Antibody (5D911) is a Mouse antibody targeting PKM. Anti-PKM Antibody (5D911) can be used in ELISA, WB, IHC, IF, FC, IP.

IgG1

5D911

Human, Mouse

1. Western Blot
-Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, Jurkat whole cell lysate
-All lanes: PKM antibody at 1:5000
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 58 kDa
-Observed band size: 58 KDa
-Exposure time: 1min
2. Western Blot
-Positive WB detected in: Mouse Brain tissue, Mouse Skeldtal Muscle tissue
-All lanes: PKM antibody at 1:1000
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 58 kDa
-Observed band size: 58 KDa
-Exposure time: 5min
3. Western Blot
-Positive WB detected in: MCF-7 whole cell lysate at 40µg, 20µg, 10µg, 5µg, 2.5µg, 1.25µg, 0.625µg
-All lanes: PKM antibody at 1:5000
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 58 kDa
-Observed band size: 58 KDa
-Exposure time: 5min
4. Western Blot
-Positive WB detected in: MCF-7 whole cell lysate
-All lanes: PKM antibody at 1:4000, 1:8000, 1:16000, 1:32000, 1:64000, 1:128000, 1:256000, 1:512000
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 58 kDa
-Observed band size: 58 KDa
-Exposure time: 5min
5. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
6. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
7. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
8. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human lung cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
9. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human lung cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
10. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human lung cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
11. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
12. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
13. IHC image of TMAH-00984 diluted at 1:1000 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
14. Immunofluorescence staining of A549 cells with TMAH-00984 at 1:215, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
15. Immunofluorescence staining of Hela cells with TMAH-00984 at 1:215, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
16. Immunofluorescence staining of HepG2 cells with TMAH-00984 at 1:215, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
17. Immunoprecipitating PKM in Hela whole cell lysate
-Lane 1: Mouse control IgG instead of TMAH-00984 in Hela whole cell lysate.
-Lane 2: TMAH-00984 (1.2ul) + Hela whole cell lysate (500ug)
-Lane 3: Hela whole cell lysate (10ug)
For western blotting, the blot was detected with TMAH-00984 at 1:2000, and a HRP-conjugated Protein G antibody was used as the secondary antibody at 1:2000
18. Overlay histogram showing Hela cells stained with TMAH-00984 (red line) at 1:50. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
19. Overlay histogram showing HepG2 cells stained with TMAH-00984 (red line) at 1:50. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.

ELISA, WB, IHC, IF, FC, IP

Monoclonal

Unconjugated

Recombinant Protein: Human Pyruvate kinase PKM Protein (2-531AA)

Human

5315

Immunology