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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
InVivoMAb Anti-Human TSHR/LGR3 Antibody (K1-18)
- 抗体英文名:
InVivoMAb Anti-Human TSHR/LGR3 Antibody (K1-18)
- 浓度:
1 mg/ml
- 应用范围:
Agonist, ELISA
- 宿主:
Mouse
- 适应物种:
Human
- 保质期:
1 year
- 级别:
科研级
- 库存:
999
- 供应商:
AntibodySystem
- 克隆性:
Monoclonal
- 亚型:
IgG2a, kappa
- 规格:
100ug

| 宿主 | Mouse |
| 种属反应性 | Human |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4. |
| 浓度 | 1 mg/ml |
| 纯度 | >95% as determined by SDS-PAGE. |
| 克隆类型 | Monoclonal |
| 同种型 | IgG2a, kappa |
| 应用 | Agonist, ELISA |
| 靶标 | Thyroid-stimulating hormone receptor, TSH-R, TSHR, Thyrotropin receptor, LGR3 |
| 纯化方式 | Protein A/G purified from cell culture supernatant. |
| 内毒素水平 | Please contact with the lab for this information. |
| Accession号 | P16473 |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| 克隆号 | K1-18 |
| 备注 | For research use only. Not suitable for clinical or therapeutic use. |
AntibodySystem's product range supports research in multiple fields, encompassing 48 types of viruses, superbugs, parasites, oncology, Alzheimer's, Parkinson's, hypersensitivity, immune suppression, and immune activation.
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文献和实验Simultaneous Quantification of t(14;18) and HPRT Exon 2/3 Deletions in Human Lymphocytes
measures the frequency of t(14;18) translocations that result in the dysfunctional regulation of the antiapoptotic gene BCL-2 . The other assay measures the frequency of a deletion caused by illegitimate V(D)J recombination in the X-linked HPRT gene.
[欢迎下载]:Antibody Engineering: Methods and Protocols
. coli 15 Expression of Recombinant Antibodies in Mammalian Cell Lines 16 Human Antibody Production Using Insect-Cell Expression Systems 17 Antibody Production in Transgenic Plants 18 Directed Mutagenesis of Antibody Variable Domains 19 Antibody
(1 ). In our laboratory, we have developed methods to immortalize specific antibody-producing cells by fusing secreting EBV-activated lymphocytes to mouse-human heteromyeloma cell lines with electrofusion, followed by cloning (2 ). This methodology has allowed
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