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小鼠胰岛素样生长因子结合蛋白1 IGFBP-1

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  • 公司名称北京方程嘉鸿科技有限公司
  • 品       牌
  • 型       号
  • 所  在  地北京市
  • 厂商性质经销商
  • 更新时间2017/4/6 23:34:38
  • 访问次数98
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小鼠胰岛素样生长因子结合蛋白1 IGFBP-1 产品信息

试剂盒名称:小鼠胰岛素样生长因子结合蛋白1 IGFBP-1

Pig Melanotransferrin (MFI2) ELISA

规格: 96T/48T
品牌:BIOFINE
种属:人ELISA试剂盒
检测波长:450nm
所需样本体积: 50-100ul
适用范围:仅供科研
保存及有效期:2-8℃,六个月,-20℃一年
检测目的:用于测定血清,血浆及相关液体小鼠胰岛素样生长因子结合蛋白1 IGFBP-1含量。适合检测包括血清、血浆、尿液、胸腹水、灌洗液、脑脊液、细胞培养上清、组织匀浆等标本。
 

1.提供全程(售前,售后)提供技术指导,免除您实验的后顾之忧。2.试剂盒*保障,有质量问题,免费包退换。3.提供免费代测服务,让您省时省心。4.送货上门,和各大快递公司都有合作,保证发货及时,运输无忧。

 

contains 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]

 

猪外切酶体成分2(EXOSC2)检测盒Pig Exosome Component 2 (EXOSC2) ELISA

人多功能蛋白聚糖(VS)测定盒Human Versican (VS) ELISA

人干扰素α8(IFNα8)测定盒Human Interferon Alpha 8 (IFNa8) ELISA

猪PRMT5协同因子(COPR5)检测盒Pig Cooperator Of PRMT5 (COPR5) ELISA

人神经型一氧化氮合酶()测定盒Human Nitric Oxide Synthase 1, Neuronal () ELISA

人聚集蛋白聚糖(AGC)测定盒Human Aggrecan (AGC) ELISA

猪血清淀粉样蛋白A(SAA)检测盒Pig Serum Amyloid A (SAA) ELISA

猪肽基脯氨酰异构酶C(PPIC)检测盒Pig Peptidylprolyl Isomerase C (PPIC) ELISA

猪肿瘤坏死因子受体超家族成员1A(TNFRSF1A)检测盒Pig Tumor Necrosis Factor Receptor Superfamily, Member 1A (TNFRSF1A) ELISA

猪干扰素诱导T-细胞α亚族趋化剂(ITαC)检测盒Pig Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) ELISA

猪D-二聚体(D2D)检测盒Pig D-Dimer (D2D) ELISA

猪血管生成素样蛋白4(ANGPTL4)检测盒Pig Angiopoietin Like Protein 4 (ANGPTL4) ELISA

 

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