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- 详细信息
- 文献和实验
- 技术资料
- 亚型:
IgG1, kappa
- 形态:
Liquid
- 保存条件:
-20°C
- 克隆性:
单克隆
- 适应物种:
Hepatitis C virus genotype 1a (isolate H77) (HCV) & Hepatitis C virus genotype 2b (isolate HC-J8) (HCV)
- 保质期:
12 months
- 级别:
一抗
- 供应商:
武汉益普生物科技有限公司
- 宿主:
Human
- 应用范围:
ELISA, Neutralization
- 抗体英文名:
Anti-HCV NS1/gp68/gp70/Envelope glycoprotein E2 Antibody (E6.D10)
- 规格:
50μg/100μg/1mg
| 规格: | 50μg | 产品价格: | ¥1350.0 |
|---|---|---|---|
| 规格: | 100μg | 产品价格: | ¥2300.0 |
| 规格: | 1mg | 产品价格: | ¥11160.0 |
| 产品名 | Anti-HCV NS1/gp68/gp70/Envelope glycoprotein E2 Antibody (E6.D10) |
| 货号 | RVV08619 |
| 靶标 | NS1, gp68, gp70, Envelope glycoprotein E2, Genome polyprotein |
| 克隆号 | E6.D10 |
| 克隆类型 | Monoclonal |
| 同种型 | IgG1, kappa |
| 宿主 | Human |
| 种属反应性 | Hepatitis C virus genotype 1a (isolate H77) (HCV) & Hepatitis C virus genotype 2b (isolate HC-J8) (HCV) |
| 应用 | ELISA, Neutralization |
| 纯度 | >95% as determined by SDS-PAGE. |
| 内毒素水平 | Please contact with the lab for this information. |
| 纯化方式 | Protein A/G purified from cell culture supernatant. |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4. |
| 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. |
| 说明 | For research use only. |

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文献和实验Anticardiolipin Antibody and Anti-beta 2 Glycoprotein I Antibody Assays
) antibodies and anti-beta 2 glycoprotein I (β2-GPI) antibodies. Other autoantibodies, such as those directed against anionic phospholipids, can also be assayed; however they are not of clinical significance. Participation in a quality assurance
Flow Cytometric Measurement of Functional and Phenotypic P-Glycoprotein
rhodamine 123, an assay for daunorubicin accumulation, and an assay to measure P-glycoprotein levels using the MRK16 antibody. Our protocols include the use of an anti-CD45 antibody for the identification of leukemic blasts. The protocols described
of the quasispecies is important. The hypervariable region 1 (HVR1) of the E2 glycoprotein has been particularly well studied in this regard. We present here a rapid method for characterizing the HVR1 quasispecies, based on in vitro coupled transcription/translation
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