- ￥5000
- GeneTex
- 美国
- GTX02123
- 2025年07月03日
- ICC/IF, FACS
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant Human CXADR / CAR protein
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 适应物种：
Human
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX02123
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
ICC/IF, FACS
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
Coxsackie Adenovirus Receptor
- 抗体英文名：
Coxsackie Adenovirus Receptor antibody [271]
- 抗体名：
Coxsackie Adenovirus Receptor 抗体 [271]
- 规格：
100 μl
FACS analysis of HT-29 cells using GTX02123 Coxsackie Adenovirus Receptor antibody [271].
The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.
ICC/IF analysis of PFA-fixed U2OS cells using GTX02123 Coxsackie Adenovirus Receptor antibody [271].
Red : Primary antibody
Blue : DAPI
Dilution : 1:60
Permeabilzation : 0.3% Triton X-100
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文献和实验Transfection Complexes Generated with Adenovirus and Polyethylenimine-Condensed DNA
to receptor-mediated gene delivery (5 ). A number of permeabilizing agents have now been used to enhance gene transfer, but adenovirus is by far the most potent (6 ,7 ). The augmentation of DNA delivery by adenovirus particles is primarily
Strategies to Adapt Adenoviral Vectors for Targeted Delivery
in other tissues. The use of recombinant adenoviruses as vectors for gene therapy is restricted by the widespread distribution of the coxsackie and adenovirus receptor (CAR) (1 ,2 ), which allows infection of a range of tissues and precludes specific in vivo
Use of Mesenchymal Stem Cells for Gene Delivery to Intracranial Glioma
-adenovirus receptor. This chapter describes in detail how such adenoviral transduction of MSCs mediated by cell-permeable peptides should be prepared and handled, and applied for the use of targeted therapeutic gene delivery into glioma by an in vitro
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