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Reg3g抗体Reg3g兔多抗抗体Regenerating
islet-derived protein 3-gamma 15 kDa form] antibody抗体Reg3g Antibody, Biotin conjugated抗体- ￥880 - 1320
- CUSABIO
- CN
- CSB-PA019549LD01RA
- 2025年07月16日
- ELISA
- Rabbit
- Rat
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- 文献和实验
- 技术资料
- 免疫原：
Recombinant Rat Regenerating islet-derived protein 3-gamma protein (27-174AA)
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
Polyclonal
- 标记物：
Biotin
- 适应物种：
Rat
- 保质期：
6个月
- 抗原来源：
Rattus norvegicus (Rat)
- 目录编号：
P42854
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA
- 浓度：
>95%,Protein G purified
- 靶点：
Reg3g
- 抗体英文名：
Reg3g Antibody, Biotin conjugated
- 抗体名：
Regenerating islet-derived protein 3-gamma 15 kDa form] antibody
- 规格：
100μg/50μg
| 规格： | 100μg | 产品价格： | ￥1320.0 |
|---|---|---|---|
| 规格： | 50μg | 产品价格： | ￥880.0 |
保存缓冲液
Preservative: 0.03% Proclin 300Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
功能
Bactericidal C-type lectin which acts exclusively against Gram-positive bacteria and mediates bacterial killing by binding to surface-exposed carbohydrate moieties of peptidoglycan. Restricts bacterial colonization of the intestinal epithelial surface and consequently limits activation of adaptive immune responses by the microbiota. The uncleaved form has bacteriostatic activity, whereas the cleaved form has bactericidal activity against L.monocytogenes and methicillin-resistant S.aureus. Regulates keratinocyte proliferation and differentiation after skin injury (By similarity).风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验to protein occurs. Both hydrophobic and ionic interactions stabilize the anionic form of the dye, causing a visible color change. The assay is useful since the extinction coefficient of a dye-albumin complex solution is constant over a 10-fold concentration
Identifying Protein Interactions by Hydroxyl‐Radical Protein Footprinting
protein footprinting is a straightforward and direct method to map protein sites involved in macromolecular interactions. The first step is to radioactively end?label the protein. Using hydroxyl radicals as a peptide backbone cleavage reagent, the protein
Use of Flow Cytometric Methods to Quantify Protein‐Protein Interactions
that is compatible for high?throughput screening is also provided. Curr. Protoc. Cytom. 51:13.11.1?13.11.15. © 2010 by John Wiley & Sons, Inc. Keywords: RGS; G protein; protein?protein interaction; FCPIA; high?throughput screening; multiplexing
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