Anti-PTH1R Antibody

筛选器： All WB FCM ELISA

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  Western blot analysis of PTH1R using anti-PTH1R antibody (A01588). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: 293T whole cell lysates,
  Lane 2: HepG2 whole cell lysates,
  Lane 3: HUH-7 whole cell lysates,
  Lane 4: monkey COS-7 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PTH1R antigen affinity purified polyclonal antibody (A01588) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for PTH1R at approximately 66 kDa. The expected band size for PTH1R is at 66 kDa.

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  Flow Cytometry analysis of HEL cells using anti-PTH1R antibody (A01588).
  Overlay histogram showing HEL cells stained with A01588 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PTH1R Antibody (A01588) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Western blot analysis of PTH1R using anti-PTH1R antibody (A01588). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: 293T whole cell lysates,
  Lane 2: HepG2 whole cell lysates,
  Lane 3: HUH-7 whole cell lysates,
  Lane 4: monkey COS-7 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PTH1R antigen affinity purified polyclonal antibody (A01588) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for PTH1R at approximately 66 kDa. The expected band size for PTH1R is at 66 kDa.

• 

  Flow Cytometry analysis of HEL cells using anti-PTH1R antibody (A01588).
  Overlay histogram showing HEL cells stained with A01588 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PTH1R Antibody (A01588) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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