- ￥5600
- GeneTex
- 美国
- GTX85047
- 2025年07月14日
- WB, IHC-P, ELISA
- Rabbit
- Human, Mouse, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Nhe-1 antibody was raised against a 20 amino acid synthetic peptide near the carboxy terminus of the human Nhe-1.The immunogen is located within the last 50 amino acids of Nhe-1.
- 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：
Polyclonal
- 标记物：
Unconjugated
- 适应物种：
Human, Mouse, Rat
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX85047
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, IHC-P, ELISA
- 浓度：
1 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
NHE-1
- 抗体英文名：
NHE-1 antibody
- 抗体名：
NHE-1 抗体
- 规格：
100 μg
WB analysis of rat kidney tissue lysate using GTX85047 NHE-1 antibody.
Working concentration : (A) 1 and (B) 2 μg/ml
IHC-P analysis of human brain tissue using GTX85047 NHE-1 antibody.
Working concentration : 2.5 μg/ml
IHC-P analysis of human brain tissue using GTX85047 NHE-1 antibody.
Working concentration : 20 μg/ml
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文献和实验Singh Y et al., J Biol Chem 2016 (PMID:27629415)
Abdelazeem KNM et al., Cell Physiol Biochem 2017 (PMID:28467979)
Gene Transfer in Vascular Cells Using an Engineered Na-H Exchanger (NHE1) as a Selectable Marker
The techniques of gene transfer using transfection via electroporation, CaPO4 , or cationic lipids rely on selectable markers because of the low efficiency of this approach. Selectable markers range from fluorescent molecules to a variety
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera
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