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當前位置:北京方程嘉鴻科技有限公司>>ELISA試劑盒>>人ELISA試劑盒科研用>>小鼠熱休克蛋白90 HSP-90代檢測

小鼠熱休克蛋白90 HSP-90代檢測

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代檢測小鼠熱休克蛋白90 HSP-90的老師請務認真填寫樣本登記單,并將實驗要求及時告知銷售人員

詳細介紹

試劑盒名稱:小鼠熱休克蛋白90 HSP-90代檢測

Pig Beta Hydroxybutyric Acid (OHb) ELISA

規格: 96T/48T
品牌:BIOFINE
種屬:人ELISA試劑盒
檢測波長:450nm
所需樣本體積: 50-100ul
適用范圍:僅供科研
保存及有效期:2-8℃,六個月,-20℃一年
檢測目的:用于測定血清,血漿及相關液體小鼠熱休克蛋白90 HSP-90含量。適合檢測包括血清、血漿、尿液、胸腹水、灌洗液、腦脊液、細胞培養上清、組織勻漿等標本。
 

1.提供全程(售前,售后)提供技術指導,免除您實驗的后顧之憂。2.試劑盒*保障,有質量問題,免費包退換。3.提供免費代測服務,讓您省時省心。4.送貨上門,和各大快遞公司都有合作,保證發貨及時,運輸無憂。

 

小鼠熱休克蛋白90 HSP-90contains the standard concentration of analyte will be prepared. Unknowns that generate a signal that is stronger than the known sample are "positive." Those that generate weaker signal are "negative." Doctor Dennis E Bidwell and Alister Voller created the test. History Before the development of the ELISA, the only option for conducting an immunoassay was radioimmunoassay, a technique using radioactively-labeled antigens or antibodies. In radioimmunoassay, the radioactivity provides the signal, which indicates whether a specific antigen or antibody is present in the sample. Radioimmunoassay was first described in a paper by Rosalyn Sussman Yalow and Solomon Berson published in 1960.[5] Because radioactivity poses a potential health threat, a safer alternative was sought. A suitable alternative to radioimmunoassay would substitute a non-radioactive signal in place of the radioactive signal. When enzymes (such as peroxidase) react with appropriate substrates (such as ABTS or 3,3’,5,5’-Tetramethylbenzidine), a change in color occurs, which is used as a signal. However, the signal has to be associated with the presence of antibody or antigen, which is why the enzyme has to be linked to an appropriate antibody. This linking process was independently developed by Stratis Avrameas and G.B. Pierce.[6] Since it is necessary to remove any unbound antibody or antigen by washing, the antibody or antigen has to be fixed to the surface of the container; i.e., the immunosorbent has to be prepared. A technique to accomplish this was published by Wide and Jerker Porath in 1966.[7] In 1971, Peter Perlmann and Eva Engvall at Stockholm University in Sweden, and Anton Schuurs and Bauke van Weemen in The Netherlands independently published papers that synthesized this knowledge into methods to perform EIA/ELISA.[8][9]

 

小鼠熱休克蛋白90 HSP-90代檢測

人白介素6(IL6)測定盒Human Interleukin 6 (IL6) ELISA

豬YY肽(PYY)檢測盒Pig Peptide YY (PYY) ELISA

人分泌型免疫球蛋白A(sIgA)測定盒Human Secretory Immunoglobulin A (sIgA) ELISA

人煙堿型*受體α1(CHRNα1)測定盒Human Cholinergic Receptor, Nicotinic, Alpha 1 (CHRNa1) ELISA

豬膽鹽依賴性脂肪酶(BSDL)檢測盒Pig Lipase, Bile Salt Dependent (BSDL) ELISA

豬高密度脂蛋白(HDL)檢測盒Pig High Density Lipoprotein (HDL) ELISA

人細胞附著蛋白交換因子相互作用蛋白1(IPCEF1)測定盒Human Interaction Protein For Cytohesin Exchange Factors 1 (IPCEF1) ELISA

豬攝食抑制因子1(NES1)檢測盒Pig Nesfatin 1 (NES1) ELISA

豬基質金屬蛋白酶3(MMP3)檢測盒Pig Matrix Metalloproteinase 3 (MMP3) ELISA

豬熱休克蛋白β2(HSPβ2)檢測盒Pig Heat Shock Protein Beta 2 (HSPb2) ELISA

人粘蛋白5AC(MUC5AC)測定盒Human Mucin 5 Subtype AC (MUC5AC) ELISA

人血清淀粉樣P物質(SAP)測定盒Human Serum Amyloid P Component (SAP) ELISA

 


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