细胞计数试剂盒-8（CCK-8）是一种即用型的单瓶溶液，可快速、可靠地测量各种化学物质对细胞存活率和毒性的敏感度。
超级热启动SYBR Green qPCR Master Mix是一种现成的qPCR混合物。
是基于鲁米诺底物的化学发光试剂盒，用于检测辣根过氧化物酶(HRP)标记的抗体及其关联的抗原。
BCA Protein Assay Kit是一种即用型总蛋白含量测定试剂盒，检测范围20-2000μg/mL。
磷酸酶抑制剂混合物I可以有效地抑制碱性磷酸酶和丝氨酸/苏氨酸蛋白质磷酸酶，如PP1和PP2A。
蛋白酶抑制剂混合物被用于细胞裂解液或组织提取物中，以增加蛋白质的稳定性。
广泛用于报告基因检测、蛋白质激酶实验、免疫测定和蛋白质纯化的裂解液和洗涤缓冲液
Annexin V-FITC/PI Apoptosis Detection Kit是一种使用FITC标记的Annexin V蛋白来检测细胞凋亡水平的凋亡检测类试剂盒。
细胞计数试剂盒-8（CCK-8）是一种即用型的单瓶溶液，可快速、可靠地测量各种化学物质对细胞存活率和毒性的敏感度。
超级热启动SYBR Green qPCR Master Mix是一种现成的qPCR混合物。
是基于鲁米诺底物的化学发光试剂盒，用于检测辣根过氧化物酶(HRP)标记的抗体及其关联的抗原。
BCA Protein Assay Kit是一种即用型总蛋白含量测定试剂盒，检测范围20-2000μg/mL。
磷酸酶抑制剂混合物I可以有效地抑制碱性磷酸酶和丝氨酸/苏氨酸蛋白质磷酸酶，如PP1和PP2A。
蛋白酶抑制剂混合物被用于细胞裂解液或组织提取物中，以增加蛋白质的稳定性。
广泛用于报告基因检测、蛋白质激酶实验、免疫测定和蛋白质纯化的裂解液和洗涤缓冲液
Annexin V-FITC/PI Apoptosis Detection Kit是一种使用FITC标记的Annexin V蛋白来检测细胞凋亡水平的凋亡检测类试剂盒。
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Therapeutic targeting of the DDR1–NF-κB–NRF2 axis inhibits PDAC growth and metabolism. a, Parental and E79Q KPC cells plated on wild-type or R/R ECM were incubated in LG medium with or without 7rh, ML120B or ML385. Total viable cells are presented relative to parental cells that were treated with vehicle and plated on wild-type ECM.
The effect of glycerophospholipids on CD8+ T cells. (B) Migration of colon tumor cells after glycerophospholipid treatment.
Construction and characterization of the FEMMAN chip. e, Fluorescence images of Cy5 on pGOLD substrate at (1) 200 pM, (2) 20 pM, (3) 2 pM, and (4) 200 fM compared to a quartz substrate at (5) 200 pM and (6) 20 pM. The Cy5 fluorophore density at 20 pM on both the (7) plasmonic substrate and (8) the quartz substrate was comparable.
(F-G)Western blotting and quantification analyses of the effect of GPRC5A overexpression on LAMTOR1 stability in TNBC cells.
PAD@MS improves tumor immunogenicity to activate immune response. B) CLSM imaging of CRT on the surface of MC38 tumor cells after treatments.
KT-NE reactivates dysfunctional TIDCs. (E) Representative fluorescent images and (F) quantification of GLUT1-based glucose uptake via 2-NBDG staining.
Excessive oxidative stress and ER stress induce lipid-laden TIDCs malfunction. (E) Intracellular lipid content was assessed via BODIPY 493/503 staining in TIDCs and DCs from normal culture medium.
Intracellular ferroptosis evaluations. d) CLSM images of C11-BODIPY581/591-stained 4T1 cells after CMS treatment (scale bar = 20 μm).
