Human Major Facilitator Superf
amily Domain Containing Protein 2A (MFSD2A) ELISA Kit试剂盒，orb781459，biorbyt- ￥3900
- biorbyt
- 0.63-40 ng/mL
- 0.239 ng/mL
- orb781459
- 英国
- 2026年01月22日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
999
- 供应商：
biorbyt
- 检测范围：
0.63-40 ng/mL
- 检测方法：
Sandwich
- 应用：
ELISA
- 适应物种：
Human
- 样本：
Tissue homogenates, cell lysates and other biological fluids
- 灵敏度：
0.239 ng/mL
- 规格：
48 T
产品别名：MFSD2 ELISA Kit, NLS1 ELISA Kit, Sodium-dependent lysophosphatidylcholine symporter 1 ELISA Kit
应用笔记：standard: 40 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human MFSD2A. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MFSD2A. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human MFSD2A, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human MFSD2A in the samples is then determined by comparing the OD of the samples to the standard curve
实验时长：3.5h
UniProt ID:Q8NA29
Note：For research use only.
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文献和实验Mapping Protein‐Protein Interactions with Phage‐Displayed Combinatorial Peptide Libraries
Figure 17.4.1 Photograph of a phage ELISA result. Using eight different clones that were isolated with GST‐SrcSH3 domain as the target, 25 µl of culture supernatant were added to pairs of microtiter plate wells containing GST‐SrcSH3 or GST
Figure 2.12.1 MnM Input page, which is used to enter queries. Simplified instructions for entering a query are numbered. Queries can be either a RefSeq accession number (2a) or a protein sequence (2b).
-derived, protein containing blocking agents often face problems in modern diagnostic assays. As discussed earlier, proteins from the blocking layer can be targets of patient antibodies or, due to the often promiscuous nature of protein interactions
