Western blot analysis of immunoprecipitates from c-Myc-tagged protein using c-Myc-tag Antibody, pAb, Rabbit (Cat. No. A00172).
Lane 1: c-Myc tagged fusion protein as control.
Lane 2: Immunoprecipitates of c-Myc tagged fusion protein incubated with Rabbit IgG Control (GenScript, Cat. No. A01008) and Protein A served as negative control
Lane 3: Immunoprecipitates of c-Myc tagged fusion protein incubated with c-Myc-tag Antibody, pAb, Rabbit (GenScript, A00172) and Protein A.
The signal was developed with IRDyeTM800 Conjugated affinity Purified Goat Anti-Rabbit IgG.
Western blot analysis of c-Myc tagged fusion proteins expressed in E. coli cell lysate using c-Myc-tag Antibody (GenScript, A00172, 1 µg/ml)
The signal was developed with IRDyeTM 800 Conjugated Goat Anti-Rabbit IgG.
Western blot analysis of c-Myc fusion protein (MW≈52KD) using 1 µg/ml Rabbit Anti-c-Myc-tag Polyclonal Antibody (GenScript, A00172)
Lane 1-3: c-Myc fusion protein in HEK293 cell lysate
Lane 4: Negative HEK293 cell lysate
Secondary antibody: Goat Anti-Rabbit IgG (H&L) [HRP] Polyclonal Antibody (GenScript, A00098, 1:20,000)
The signal was developed with LumiSensorTM HRP Substrate Kit (GenScript, L00221V500)
Customer Reviews:
c-Myc-tag Antibody, pAb, Rabbit (GenScript,A00172) were used in western blotting to show overexpression of Bik1, Pac1, or Dyn1 by GAL1 promoter in budding yeast.
Left and middle:
Western blot of cell lysates prepared from strains with either endogenous or GAL1 promoter driving expression of indicated 13myc-tagged gene.
Right:
Western blot of Dyn1-13myc protein in strains with either the endogenous or GAL1 promoter driving the expression of PAC1 or BIK1.
For all blots, equal amount of total cell lysate was loaded in each lane, transferred to PVDF and probed with anti-c-Myc antibody(GenScript, A00172).
All strains were grown to mid-log phase in SD media supplemented with 2% galactose, and then harvested.
c-Myc-tag Antibody, pAb, Rabbit
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A00172 |
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¥990 |
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联系黄金城集团 |