SMAD1/SMAD5/SMAD9 Polyclonal
Antibody（多克隆抗体） | SMAD1/SMAD5/SMAD9 Antibody | SMAD1/SMAD5/SMAD9抗体- ￥880 - 1320
- CUSABIO
- 武汉
- CSB-PA004105
- 2026年03月28日
- ELISA, WB, IHC
- Rabbit
- Human, Mouse, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Synthesized peptide derived from the N-terminal region of Human Smad1/5/9.
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
-20°C or -80°C
- 克隆性：
多克隆
- 标记物：
Non-conjugated
- 适应物种：
Human, Mouse, Rat
- 抗原来源：
12个月
- 目录编号：
Homo sapiens (Human)
- 供应商：
武汉研升生物科技有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA, WB, IHC
- 靶点：
SMAD1/SMAD5/SMAD9
- 抗体英文名：
SMAD1/SMAD5/SMAD9 Antibody
- 抗体名：
SMAD1/SMAD5/SMAD9 Antibody
- 规格：
100μg/50μg
| 规格： | 100μg | 产品价格： | ￥1320.0 |
|---|---|---|---|
| 规格： | 50μg | 产品价格： | ￥880.0 |
|
Product Name |
SMAD1/SMAD5/SMAD9 Antibody |
|
Code |
CSB-PA004105 |
|
Aliases |
SMAD1; BSP1; MADH1; MADR1; Mothers against decapentaplegic homolog 1; MAD homolog 1; Mothers against DPP homolog 1; JV4-1; Mad-related protein 1; SMAD family member 1; SMAD 1; Smad1; hSMAD1; Transforming growth factor-beta-signaling protein |
|
Product Type |
Polyclonal Antibody |
|
Immunogen Species |
Homo sapiens (Human) |
|
Size |
100μg/50μg |
|
Uniprot ID |
Q15797/Q99717/O15198 |
|
Immunogen |
Synthesized peptide derived from the N-terminal region of Human Smad1/5/9. |
|
Host Species |
Rabbit |
|
Species Reactivity |
Human, Mouse, Rat |
|
Tested Applications |
WB, IHC, ELISA |
|
Clonality |
Polyclonal |
|
Isotype |
IgG |
|
Conjugate |
Non-conjugated |
|
Buffer |
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
|
Form |
Liquid |
|
Stroage |
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
|
Purification Method |
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
|
Target Names |
SMAD1/SMAD5/SMAD9 |
|
Research Areas |
Epigenetics and Nuclear Signaling;Cancer;Signal transduction；Stem cells |
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a subset of genomic DNA sequences of type 5'-(NNN )3 -3', whereas the 6ZF library would recognize a subset of genomic sequences of type 5'-(NNN )6 -3'. Given the zinc-finger domains used, both libraries were more likely to recognize (RNN)x -type sequences
Phage‐Based Expression Cloning to Identify Interacting Proteins
the interacting protein. This technique leads directly to the isolation of a cDNA encoding the interacting protein, bypassing the need for labor?intensive protein purification, microsequencing, or antibody production.
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