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abs830032-50uL 现货
¥800.00
129 .00
abs830032-100uL 现货
1200 .00
abs830032-500uL 2-3天
3800 .00
abs830032-1mL 1-2周
6200 .00
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实验结果图
1.Load 20ug total protein per lane on a standard sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). 2.Add anti-β-tubulin monoclonal antibody to a final concentration of 1-0.1μg/ml to the blot in 1×TBS-T and incubate with agitation for 30 minutes at room temperature. 3.The positive result could be visualized on the Western Blot when the concentration of anti-β-tubulin monoclonal antibody is 0.5-0.1μg/ml.
文献相关图
Positive additive effect comparison of mCIM and TCIM with 1 l of test bacteria and 10 l of test bacteria added for the 83 carbapenemase-producing strains of A. baumannii complex. The box plots demonstrated the diameters of inhibition zone around the disks in mCIM-1 l, TCIM-1 l, mCIM-10, and TCIM-10.
来源于《Journal of molecular and cellular cardiology》
Expression levels of CD44 in glioma tissues. (A) Expression patterns of CD44 in different grade glioma tissues were analyzed by reverse-transcription quantitative PCR. (B) The protein expression levels of CD44 in patients with different grade glioma tissues were analyzed by western blotting. The numbers under the blot represents the protein expression levels of CD44 in glioma tissues of different grades relative to the respective GAPDH loading controls. * P<0.05,** P<0.01.
来源于《J Cell Physiol》
F. ERK and phosphorylated (Phospho-) Erk1/2 were detected by western blot. The B16-F10 cells were treated with vehicle, lenvatinib (1000 nM, 300 nM, 100 nM) or lenvatinib plus NK cell depletion antibody (PK136, 100 μg/mL) for 4 hours. Total protein was extracted. ERK and phosphorylated (Phospho-) Erk1/2 were detected by western blot. The experiment was repeated for three times. The results are consistent. Representative results of one independent experiment are shown. *P<0.05, **P<0.01.
来源于《Experimental and Therapeutic Medicine》
Western blotting and its quantification of adipocyte-specific genes ACC, LPL, and PPARG insBMSCs transfected with pcDNA-HOXC10 or pcDNA3.1(+).
来源于《STEM CELLS DEV》
Western blotting verification of si-Plk3 knockdown efficiency of DU145 cells.
来源于《Cancer Manag Res》
来源于《cellular & molecular immunology》 DOI:10.1038/s41423-026-01414-x
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