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品牌: BD Pharmingen








反应种属:
Human (QC Testing), Rhesus, Cynomolgus, Baboon (Tested in Development)
Human (QC Testing), Rhesus, Cynomolgus, Baboon (Tested in Development)
产品介绍
产品信息
抗原名称
IFN-γ

简单描述
The BD™ CBA Human IFN-γ Flex Set is a bead-based immunoassay capable of measuring human interferon-γ (IFN-γ) in serum, plasma, and cell culture supernatant samples. Human and non-human primate reactivity was determined by testing samples with the BD CBA Human IFN-γ Flex Set. The biology and function of IFN-γ has been extensively reviewed in the literature. For more information on bead-based immunoassays, refer to the product insert for the BD CBA Human Soluble Protein Master Buffer Kit (Cat. No. 558264 or 558265).

商品描述
The BD™ CBA Human IFN-γ Flex Set is a bead-based immunoassay capable of measuring human interferon-γ (IFN-γ) in serum, plasma, and cell culture supernatant samples. Human and non-human primate reactivity was determined by testing samples with the BD CBA Human IFN-γ Flex Set. The biology and function of IFN-γ has been extensively reviewed in the literature. For more information on bead-based immunoassays, refer to the product insert for the BD CBA Human Soluble Protein Master Buffer Kit (Cat. No. 558264 or 558265).

克隆号
(RUO)

BD化合物表
- 描述数量/尺寸零件号EntrezGene ID
- Human IFN-γ Capture Bead E71 Vial(s) (1 ea)51-9005281N/A
- Human IFN-γ PE Detection ReagentN/A51-9004031N/A
- Human IFN-γ Standard1 Vial(s) (2 ea)51-9003507N/A
应用
反应种属
Human (QC Testing), Rhesus, Cynomolgus, Baboon (Tested in Development)

目标/特异性
IFN-γ

参考图片
Figure 1. Example BD CBA Human IFN-γ Flex Set standard curve. Data acquired on a BD FACSArray bioanalyzer and analzed using FCAP Array Software.
Table 1. Reproducibility: The inter-assay and intra-assay reproducibility were determined for the BD CBA Human IFN-γ Flex Set by evaluating ten replicates of three different sample levels (inter-assay) and two replicates of three different sample levels from four separate experiments (intra-assay) respectively.
Table 3. Linearity: Cell culture supernatant, 1:4 diluted serum, or 1:4 diluted EDTA-treated plasma were spiked with protein and serially diluted. The diluted samples were assayed and the results were compared with the original spiked sample.
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