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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
peptide
- 亚型:
IgG1
- 形态:
Liquid
- 保存条件:
-20℃
- 克隆性:
mAb
- 适应物种:
Human
- 保质期:
1年
- 目录编号:
TD-31494
- 级别:
科研级
- 库存:
88
- 供应商:
武汉天德
- 宿主:
Mouse
- 应用范围:
WB、ELISA、FCM
- 靶点:
详询
- 抗体英文名:
Mouse Monoclonal Antibody to CD57
- 抗体名:
CD57
- 规格:
100ul/50ul
| 规格: | 100ul | 产品价格: | ¥2180.0 |
|---|---|---|---|
| 规格: | 50ul | 产品价格: | ¥1280.0 |
Mouse Monoclonal Antibody to CD57
Description | |
| The protein encoded by this gene is a member of the glucuronyltransferase gene family. These enzymes exhibit strict acceptor specificity, recognizing nonreducing terminal sugars and their anomeric linkages. This gene product functions as the key enzyme in a glucuronyl transfer reaction during the biosynthesis of the carbohydrate epitope HNK-1 (human natural killer-1, also known as CD57 and LEU7). Alternate transcriptional splice variants have been characterized. | |
Specification | |
| Aliases | B3GAT1; NK1; HNK1; LEU7; NK-1; GLCATP; GLCUATP |
| Entrez GeneID | 27087 |
| Swissprot | Q9P2W7 |
| clone | 3F6D6 |
| WB Predicted band size | 38.3kDa |
| Host/Isotype | Mouse IgG1 |
| Antibody Type | Primary antibody |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human,Mouse,Rat,Monkey |
| Immunogen | Purified recombinant fragment of human CD57 (AA: 35-191) expressed in E. Coli. |
| Formulation | Purified antibody in PBS with 0.05% sodium azide |
Application | |
| WB | 1/500 - 1/2000 |
| FCM | 1/200 - 1/400 |
| ELISA | 1/10000 |
Product Image | |
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文献和实验CD57 分子 CD57 常用单克隆抗体或代号: Leu7,HNK- 1 主要表达细胞: NKsub,Tsub [NK] 分子质量(kDa)和结构: gp110 功 能: 参与NK活化后的杀伤作用 CD57 Aka Leu7 Glycoprotein with cell adhesion functions NK cell marker and neuroendocrine marker
16+ NK 细胞比例,并监测了细胞表面受体的差异表达,包括 CD8、CD11c、CD38、CD57 和 CD117,及其表达水平。样品制备:1. 加入 35 mL 新鲜人血(取自血库)和 20 mLPBS。2. 向 50 mL 锥形试管中加入 15 mL Ficoll-Paque,并转移 35 mL 经过 PBS 稀释的血样。3. 以室温 400 x G 持续离心试管 30 分钟。4. 用一个 (10-25 mL) 移液器或塑料的巴斯德吸管轻轻从试管中吸取间期细胞,并转移到一个新的 50 mL 锥形试管
Clonality Detection of Expanded T-Cell Populations in Patients With Multiple Myeloma
within a population of T-cells is by analysis of the length of complementarity-determining region 3 of the rearranged TCR gene, followed by sequencing. Furthermore, my colleagues and I have previously shown that the CD57+ T-cells expressing the “expanded” TCRVβ
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