【AbMole明星产品】Cell Counting Kit-8，便捷、灵敏、高文献引用

Cell Counting Kit-8试剂盒可谓是目前在细胞实验中炙手可热的一款试剂盒，常用于对细胞的增殖检测和毒性检测。相比较于往常的MTT试剂盒，CCK-8试剂盒的操作更加简便，而且灵敏度更高，因此在科研界CCK-8试剂盒一路走红，广受好评。

自AbMole推出CCK-8试剂盒以来，该产品广受全球好评。自AbMole购买使用CCK-8试剂盒发表的文献多达数十余篇，高质量的文献结果展示出了我们CCK-8试剂盒的精准度与灵敏性。

1. lncRNA H19 promotes viability and epithelial-mesenchymal transition of lung adenocarcinoma cells by targeting miR-29b-3p and modifying STAT3

实验结果展示：

Figure 4. (A) Proliferation and (B) viability were compared among pcDNA3.1-H19-, pcDNA3.-, si-H19-, si-NC-, miR-29b-3p inhibitor-, miR-29b-3p mimic-and negative control-transfected Calu-3 and NCI-H1975 cell lines. *P<0.05 vs. pcDNA3.1; #P<0.05 vs. Si-NC; @P<0.05 vs. negative control. si, short interfering; NC, negative control; miR, microRNA

Figure 8. (A) Colony formation and (B) Cell Counting Kit-8 assays were performed to determine the proliferative capacity and viability of Calu-3 and NCI-H1975 cell lines among miR-NC, miR-29b-3p mimic and miR-NC+STAT3 groups. *P<0.05 vs. miR‑29b‑3p. miR, microRNA; NC, negative control; STAT3, signal transducer and activator of transcription 3.

2. Self-implanted tiny needles as alternative to traditional parenteral administrations for controlled transdermal drug delivery

实验结果展示：

Fig. 4. In vitro testing of the SI-PI-TNs. (A) Hemolysis assay and (B) cytotoxicity of the prepared SI-PI-TNs and corresponding dissolved products at 0.2 mg/mL dose. (C) Fluorescence images of FDA (green; live cells) and PI (red; dead cells) double-stained L-929 cells treated with SI-PI-TNs at 24-72 h of incubation compared with the control group treated with PBS at 72 h of incubation. (D) In vitro drug (IVM) release profiles of TNs with or without PLGA particles.

3. Knockdown of MON1B Exerts Anti-Tumor Effects in Colon Cancer In Vitro

实验结果展示：

Figure 2. MON1B interference inhibited cell proliferation, migration, and invasion abilities of colon cancer cells. The mRNA (A) and protein levels (B) of MON1B decreased remarkably in the si-MON1B group compared with Control and NC groups. (C) Cell proliferation abilities were inhibited in a time-dependent (12, 24, and 48 h) manner in the si-MON1B group compared with Control and NC groups. (D, E) Cell migration abilities of colon cancer cells were inhibited in a time-dependent (12 and 24 h) manner in the si-MON1B group as detected by wound-healing assay. (D, F) Cell invasion abilities of colon cancer cells were significantly also inhibited. * P<0.05 and ** P<0.01 vs. Control group; # P<0.05 and ## P<0.01 vs. NC group.

Figure 3. MON1B interference inhibited cell migration and invasion abilities of colon cancer cells via inhibiting MMPs. (A-D) The mRNA levels of MMP-2, MMP-9, and MTA-1 were inhibited, while that of TIMP-2 was promoted in the si-MON1B group. (E) The protein levels of MMP-2, MMP-9, and MTA-1 were inhibited, while that of TIMP-2 was promoted in the si-MON1B group. * P<0.05 and ** P<0.01 vs. Control group; # P<0.05 and ## P<0.01 vs. NC group.

一篇又一篇的高分文献也在印证着我们cck-8试剂盒的品质，AbMole一直秉持本心，对我们的产品品质都严加把关，确保每一份试剂都合规，让您的每一个实验都无忧。