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Result
“No background detected. The antibody was highly visible in the sample. Highly specific.
In Normal NPCs and TRF2-knockdwon NPCs cells, there were target bands detected by STJ96941 Anti-β-
actin antibody (Figure: Lane1: TRF2 control NPCs; Lane 2: TRF2 knockdown NPCs).“- Sitti, Imperial College
London, United Kingdom.
Antibody Customer Review:
STJ96941 Anti-β-actin antibody
Antibody Specificity:
Antibody Rating:
Protocol
Treatment of materials: When cells were cultured to 70%-80% plating density, RIPA lysis buffer with 1:100 protease
inhibitors (Sigma) and PMSF were added. 5X loading buffer were added prior to running. No heating.
E.g. Gel electrophoresis: 12% polyacrylamide gel, constant voltage 120 V, 90 min.
Transfer: 0.45 nm PVDF membrane, wet transfer, constant voltage 20 V, 90 min.
Blocking: 1X TBST with 5% skimmed milk powder for 1 hr in room temperature.
Primary antibody probing: primary antibody was added to the solution of 1X TBST with 5% skimmed milk powder,
4˚C on roller for overnight.
Membrane wash: 1X TBST wash for 3 times at 10 minutes intervals.
Secondary antibody probing: secondary antibody was added to the solution of 1X TBST with 5% skimmed milk
powder with 1:5000 dilution ratio, for 1 hr
Membrane wash: 1X TBST wash for 3 times at 10 minutes intervals.
Visualization: ECL visualization for 1 sec.
Cell Line: Human Neural Progenitor Cells
Method of validation: Western Blot
Primary Antibody: STJ96941 Anti-β-actin antibody
Secondary Antibody
HRP goat anti-mouse, light
chain specific
Dilution ratio: 1:1000
Gel electrophoresis information:12% polyacrylamide gel, constant voltage 120 V, 90 min.
Transfer information:0.45 nm PVDF membrane, semi-dry transfer, constant voltage 20 V, 90 min.
Lane No. Antigen
Loading
amount
Primary
antibody
Primary
antibody
dilution ratio
Secondary
antibody dilution
ratio
Target band KD
Visualizati
on time
1
hESC-derived
NPCs
20ug
STJ96941
Anti-β-actin
antibody
1:1000 1:5000 ~45KD
1S
2
TRF2-
knockdown
NPCs
1S

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Western Blot Antibody Customer Review for Anti-β-actin Antibody (STJ96941)

  • 1. Result “No background detected. The antibody was highly visible in the sample. Highly specific. In Normal NPCs and TRF2-knockdwon NPCs cells, there were target bands detected by STJ96941 Anti-β- actin antibody (Figure: Lane1: TRF2 control NPCs; Lane 2: TRF2 knockdown NPCs).“- Sitti, Imperial College London, United Kingdom. Antibody Customer Review: STJ96941 Anti-β-actin antibody Antibody Specificity: Antibody Rating: Protocol Treatment of materials: When cells were cultured to 70%-80% plating density, RIPA lysis buffer with 1:100 protease inhibitors (Sigma) and PMSF were added. 5X loading buffer were added prior to running. No heating. E.g. Gel electrophoresis: 12% polyacrylamide gel, constant voltage 120 V, 90 min. Transfer: 0.45 nm PVDF membrane, wet transfer, constant voltage 20 V, 90 min. Blocking: 1X TBST with 5% skimmed milk powder for 1 hr in room temperature. Primary antibody probing: primary antibody was added to the solution of 1X TBST with 5% skimmed milk powder, 4˚C on roller for overnight. Membrane wash: 1X TBST wash for 3 times at 10 minutes intervals. Secondary antibody probing: secondary antibody was added to the solution of 1X TBST with 5% skimmed milk powder with 1:5000 dilution ratio, for 1 hr Membrane wash: 1X TBST wash for 3 times at 10 minutes intervals. Visualization: ECL visualization for 1 sec. Cell Line: Human Neural Progenitor Cells Method of validation: Western Blot Primary Antibody: STJ96941 Anti-β-actin antibody Secondary Antibody HRP goat anti-mouse, light chain specific Dilution ratio: 1:1000 Gel electrophoresis information:12% polyacrylamide gel, constant voltage 120 V, 90 min. Transfer information:0.45 nm PVDF membrane, semi-dry transfer, constant voltage 20 V, 90 min. Lane No. Antigen Loading amount Primary antibody Primary antibody dilution ratio Secondary antibody dilution ratio Target band KD Visualizati on time 1 hESC-derived NPCs 20ug STJ96941 Anti-β-actin antibody 1:1000 1:5000 ~45KD 1S 2 TRF2- knockdown NPCs 1S