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        恒遠生物小鼠腫瘤壞死因子α(TNF-α)ELISA試劑盒引用文獻
        更新時間:2023-01-09 點擊次數(shù):676


        恒遠產(chǎn)品文獻:小鼠PGE2,MMP-2,NF-κB,IL-6,TNF-α ELISA試劑盒引用文獻

        【文獻標(biāo)題】Combination of mitochondria impairment and inflammation blockade to combat metastasis

        【作者】Xiaoli Yi , Yue Yan , Lian Li , et.al

        【作者單位】四川大學(xué)(Sichuan University

        【文獻中引用產(chǎn)品】

        小鼠前列腺素E2(PGE2)ELISA試劑盒

        小鼠基質(zhì)金屬蛋白酶2(MMP-2)ELISA試劑盒

        小鼠血管內(nèi)皮細胞生長因子(VEGF)ELISA試劑盒

        小鼠鼠核因子-κBNF-κBELISA試劑盒

        小鼠白介素6(IL-6)ELISA試劑盒

        小鼠腫瘤壞死因子α(TNF-α)ELISA試劑盒

        【關(guān)鍵詞】Reactive oxygen species ,Anti-metastasis therapy ,Mitochondria impairment ,Inflammatory tumor microenvironment ,Combination therapy

        【影響因子(IF)11.4

        【出版期刊】《Journal of Controlled Release

        【產(chǎn)品原文引用】

        Prostaglandin E2 (PEG2), MMP-2, VEGF, nuclear factor-κ-gene binding (NF-κB) and interleukin 6 (IL-6) Elisa Kit was supplied by Hengyuan Technology Innovation Co., Ltd. (Shanghai, China). Other reagents were all of analytical grade or above.

        The levels of prostaglandin E2 (PGE2) in the serum was determined by a PGE2 ELISA Kit (Hengyuan technology, Shanghai, China) according to the standard protocol. Afterwards, the expression of matrix metalloproteinase (MMP- 2), interleukin (IL-6), tumor necrosis factor-α (TNF-α) and vascular

        endothelial growth factor (VEGF) in tumor tissue was quantitatively detected using ELISA kits (Hengyuan technology, Shanghai, China).

        恒遠產(chǎn)品文獻:小鼠IL-1β,TNF-α ELISA試劑盒引用文獻

        【文獻標(biāo)題】Dehydroepiandrosterone exacerbates nigericin-induced abnormal autophagy and pyroptosis via GPER activation in LPS-primed macrophages

        【作者】Ji Cao , Longlong Li, Yao Yao,et.al

        【作者單位】南京農(nóng)業(yè)大學(xué)(Nanjing Agricultural University

        【文獻中引用產(chǎn)品】

        小鼠白介素1β (IL-1β)ELISA試劑盒

        小鼠腫瘤壞死因子α(TNF-α)ELISA試劑盒

        【影響因子(IF)9.68

        【出版期刊】《Cell Death and Disease

        【產(chǎn)品原文引用】

        DHEA, dimethyl sulfoxide (DMSO), and LPS (Escherichia coli 055:B5) were provided by Sigma (St Louis, MO, USA). The fetal bovine serum (FBS) was obtained from Gibco (Erie, NY, USA). The Dulbecco's modified Eagles medium (DMEM) and trypsin-EDTA were obtained from Biological Industries (Kibbutz Beit-Haemek, Israel). Shanghai Hengyuan Biological Technology Co., Ltd. (Shanghai, China) provided the commercial mouse TNF-α and IL-1β ELISA kit. The MCE (St. Louis, MO, USA) provided the Nigericin and inhibitors that included G1, G15, MCC950, BAY11-7082, rapamycin, and compound C. The lactate dehydrogenase (LDH) activity and reactive oxygen species detection kit were provided by Beyotime Biotechnology Institute (Shanghai, China).

        恒遠產(chǎn)品文獻:小鼠IL-6,TNF-α,IL-1β,Ang 1-7,ANG-ELISA試劑盒引用文獻

        【文獻標(biāo)題】MSC-ACE2 Ameliorates Streptococcus uberis-Induced Inflammatory Injury in MammaEpithelial Cells by UpregulatinIL-10/STAT3/SOCS3 Pathway

        【作者】Shuping Yan, Chonghao Zhang, Xiaoxia Ji,et.al

        【作者單位】南京農(nóng)業(yè)大學(xué)(Nanjing Agricultural University

        【文獻中引用產(chǎn)品】

        小鼠白介素6(IL-6)ELISA試劑盒

        小鼠腫瘤壞死因子α(TNF-α)ELISA試劑盒

        小鼠白介素1β (IL-1β)ELISA試劑盒

        小鼠血管緊張素1-7Ang 1-7) ELISA試劑盒

        小鼠血管緊張素Ⅱ(ANG-)ELISA試劑盒

        【關(guān)鍵詞】S. uberis, MSC-ACE2, inflammatory injury, pyroptosis, blood-milk barrier, mammary epithelial cells

        【影響因子(IF)7.56

        【出版期刊】《Frontiers in Immunolog

        【產(chǎn)品原文引用】

        Analyzing the Concentration of IL-6,TNF-a, IL-Ib, Ang-(17), Ang II, and NAGase Activity

        In the supernatant after cell culture, IL-6, TNF-a, IL-Ib,Ang-(17), and Ang II concentrations were measured by ELISA (Hengyuan Biotechnology Co., Shanghai, China). The manufacturers instructions were followed for the ELISA test. As a unit of measurement, TNF-a, IL-Ib, Ang-(17), and Ang II

        were demonstrated as ng/L. In this case, IL-6 was demonstrated as pg/mL. Using the instructions included in the kit purchased from the Nanjing Jiancheng Bioengineering Institute (Nanjing, China), the action of NAGase was determined in the supernatant of the cell culture medium. NAGase activity was measured in units of U/L.

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