| 规格 | 价格 | 库存 |
|---|---|---|
| 25µg | ¥ 1904 | 1 |
WB -?Quality tested
ICC, IP, ICFC -?Verified
Each lot of this antibody is quality control tested by western blotting. For western blotting, the suggested use of this reagent is 0.1?- 1.0??g/mL.?For immunocytochemistry, a concentration range of 1.0?- 5.0?μg/mL is recommended.?For immunoprecipitation, the suggested use of this reagent is 2.5??g/test.?For?intracellular flow cytometric staining, the suggested use of this reagent is ≤ 0.5??g per million cells in 100 ?L volume. It is recommended that the reagent be titrated for optimal performance for each application.
This clone was tested for ICC using 4% PFA-fixed HEL cells permeabilized with either methanol or Triton X-100. While both methods were compatible with robust HEL staining, Triton X-100 permabilization resulted in stronger staining.
When using this clone for ICFC, we recommend using the True-Nuclear? Transcription Factor Buffer Set or the True Phos perm buffer. We do not recommend using the Intracellular Staining Permeabilization Wash Buffer for ICFC testing due to poor GATA1 staining.
True-Nuclear? Transcription Factor Buffer Set allowed for better binding to the epitope when compared to the True Phos perm buffer, there was a twofold difference between their median PE readings.
Erythroid and megakaryocytic cells/Nucleus