TMPRSS3抗体TMPRSS3一抗抗体Tumor-asso
ciated differentially-expressed gene 12 protein抗体TMPRSS3 Antibody抗体- ￥880 - 1320
- CUSABIO
- CN
- CSB-PA004306
- 2025年07月14日
- WB, IHC, IF, ELISA; WB:1:500-1:2000, IHC:1:100-1:300, IF:1:200-1:1000, ELISA:1:10000
- Rabbit
- Human,Mouse
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- 文献和实验
- 技术资料
- 免疫原：
Synthesized peptide derived from the C-terminal region of Human TMPRSS3.
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
/
- 标记物：
Non-conjugated
- 适应物种：
Human,Mouse
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
P57727
- 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：
WB, IHC, IF, ELISA; WB:1:500-1:2000, IHC:1:100-1:300, IF:1:200-1:1000, ELISA:1:10000
- 浓度：
>95%,The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
- 靶点：
TMPRSS3
- 抗体英文名：
TMPRSS3 Antibody
- 抗体名：
TMPRSS3;ECHOS1;TADG12;UNQ323/PRO382;Transmembrane protease serine 3;Serine protease TADG-12;Tumor-associated differentially-expressed gene 12 protein
- 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
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.功能
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文献和实验Identification and Cloning of Differentially Expressed Genes by DDRT-PCR
The invention of polymerase chain reaction (PCR) and its application to amplification of reverse transcribed cDNA copies of mRNA has opened new possibilities for the development of techniques for identification of changes in gene expression
Changes in cell behavior are driven by changes in gene expression. Thus, in order to understand the mechanisms regulating cell behavior, one has to identify and characterize differentially expressed genes. Standard methods currently used
Systemic IL-12 Gene Therapy for Treating Malignancy via Intramuscular Electroporation
of an acute dose of IL-12 protein is very costly and severely toxic. Here, a simple, economic, and less toxic approach, intramuscular administration of IL-12 gene, is provided for treating tumors in three tumor models. The results indicate that intramuscular
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