- ￥4300
- GeneTex
- 美国
- GTX23611
- 2025年07月16日
- WB, IHC-P, IHC-Fr
- Rabbit
- Human, Mouse, Rat, Frog, Squirrel
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 免疫原：
Synthetic peptides corresponding to residues C(362) W R K R Q P R (R/L) E E R K A P E S Q E D(380) of rat RAGE.
- 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, Frog, Squirrel
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Rat
- 目录编号：
GTX23611
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, IHC-P, IHC-Fr
- 浓度：
0.33 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
RAGE
- 抗体英文名：
RAGE antibody
- 抗体名：
RAGE 抗体
- 规格：
100 μl
Mouse tissue extract (50 μg) was separated by 12% SDS-PAGE, and the membrane was blotted with RAGE antibody (GTX23611) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Rat tissue extract (50 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with RAGE antibody (GTX23611) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
RAGE antibody detects RAGE protein in rat lung by immunohistochemical analysis.
Sample: Paraffin-embedded rat lung.
RAGE antibody (GTX23611) diluted at 1:400.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
IHC-P analysis of normal mouse heart tissue with (ledt) or without (right) RAGE antibody at a dilution of 1:20. Heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes.
Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min
IHC-P analysis of normal mouse kidney tissue with (ledt) or without (right) RAGE antibody at a dilution of 1:20. Heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes.
Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min
IHC-P analysis of normal mouse lymph node tissue with (ledt) or without (right) RAGE antibody at a dilution of 1:20. Heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes.
Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min
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- 作者
- 内容
- 询问日期
文献和实验Fukuoka CY et al., PLoS One 2020 (PMID:32750068)
Al-Attar R et al., Gene 2020 (PMID:32777527)
Abedini A et al., J Clin Invest 2018 (PMID:29337308)
Ono H et al., Sci Rep 2018 (PMID:30002389)
Logan SM et al., PeerJ 2018 (PMID:29888131)
Sukjamnong S et al., Am J Physiol Lung Cell Mol Physiol 2017 (PMID:28522560)
Fukuoka CY et al., PLoS One 2017 (PMID:28099448)
Saby C et al., Oncotarget 2016 (PMID:27121132)
Daffu G et al., Diabetes 2015 (PMID:26253613)
Chen YC et al., Sci Rep 2016 (PMID:26739898)
Juranek JK et al., Front Cell Neurosci 2015 (PMID:26733811)
Rai V et al., J Exp Med 2012 (PMID:23209312)
Shang L et al., PLoS One 2010 (PMID:20404919)
Lee CC et al., Biochem Pharmacol 2013 (PMID:23948063)
Rai V et al., J Biol Chem 2012 (PMID:22194616)
Pollreisz A et al., Atherosclerosis 2010 (PMID:20701913)
Ru-Jeng Teng et al., Free Radic Biol Med 2021 (PMID:33607217)
Laura Hansen et al., J Am Heart Assoc 2021 (PMID:34689598)
Lu WH et al., Toxics 2020 (PMID:32947820)
RACE and RAGE Cloning in Parasitic Microbial Eukaryotes
and RAGE, we used to successfully clone partial and full-length ORFs from amitochondriate parasitic microbial eukaryotes. The RACE approach uses cDNA as template for PCR cloning whereas RAGE uses genomic DNA. These two approaches were used to complement
Rapid Amplification of Gene Ends (RAGE) from Gene Libraries by Anchored PCR
Isolation of a full-length gene on the basis of limited sequence information is often troublesome and challenging. Tremendous effort is needed to isolate a specific gene by screening cDNA or genomic libraries by oligonucleotide or nucleic
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
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