- ￥5600
- GeneTex
- 美国
- GTX82905
- 2025年07月13日
- WB, ICC/IF, IHC-P, IHC-Fr, IP
- Rabbit
- Human, Mouse, Rat, Zebrafish, Rabbit, Bovine, Guinea pig
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Synthetic peptide corresponding to residues T(724) K R R A I G F K K L A E A V K(739) C of rat bNOS.
- 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, Zebrafish, Rabbit, Bovine, Guinea pig
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Rat
- 目录编号：
GTX82905
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, ICC/IF, IHC-P, IHC-Fr, IP
- 靶点：
This antibody does not detect endothelial NOS (eNOS) or inducible NOS (iNOS).
- 抗体英文名：
nNOS antibody
- 抗体名：
nNOS 抗体
- 规格：
100 μl
IHC-P analysis of rat cerebellum tissue using GTX82905 nNOS antibody.
Left : Primary antibody
Right : Negative control without primary antibody
Antigen retrieval : heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes
Dilution : 1:200
IHC-P analysis of mouse skeletal muscle tissue using GTX82905 nNOS antibody.
Left : Primary antibody
Right : Negative control without primary antibody
Antigen retrieval : heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes
Dilution : 1:400
WB analysis of 40 μg of mouse (Lane 1) and rat brain (Lane 2) tissue lysate using GTX82905 nNOS antibody.
Dilution : 1:1000
ICC/IF analysis of SH-SY5Y cells using GTX82905 nNOS antibody. Panel e is a no primary antibody control.
Green : Primary antibody
Blue : Nuclei
Red : Actin
Fixation : 4% PFA
Permeabilization : 0.1% Triton X-100 for 10 minute
Dilution : 1:250 dilution in 0.1% BSA and incubated for 3 hours at room temperature
IHC-P analysis of rat brain tissue using GTX82905 nNOS antibody.
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文献和实验Chou CC et al., J Cardiovasc Pharmacol 2020 (PMID:31842025)
Demirpence S et al., Curr Ther Res Clin Exp 2009 (PMID:24683224)
Cloning and Expression of Human eNOS and nNOS Using the Baculovirus-Insect Cell System
To date, the cDNAs and genes encoding three distinct forms of the enzyme nitric oxide synthase (NOS) have been described (reviewed in ref. 1 ). The family of NOS enzymes generate nitric oxide (NO) from arginine, producing citrulline
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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