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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant protein encompassing a sequence within the C-terminus region of human FAK. The exact sequence is proprietary.
- 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:
GTX100764
- 级别:
Primary Antibodies
- 库存:
Available
- 供应商:
GeneTex
- 宿主:
Rabbit
- 应用范围:
WB, ICC/IF, IHC-P
- 浓度:
1.02 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点:
FAK
- 抗体英文名:
FAK antibody
- 抗体名:
FAK 抗体
- 规格:
100 μl/25 μl
| 规格: | 100 μl | 产品价格: | ¥4000.0 |
|---|---|---|---|
| 规格: | 25 μl | 产品价格: | ¥1700.0 |
Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with FAK antibody (GTX100764) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
FAK antibody detects FAK protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded rat spleen.
FAK stained by FAK antibody (GTX100764) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
FAK antibody detects FAK protein at cytoplasm by immunohistochemical analysis.
Sample: Paraffin-embedded mouse brain.
FAK stained by FAK antibody (GTX100764) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with FAK antibody (GTX100764) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with FAK antibody (GTX100764) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
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文献和实验Hsu HY et al., Evid Based Complement Alternat Med 2012 (PMID:23320038)
Wan-Ping Su et al., Biomed Pharmacother 2023 (PMID:37196543)
Chen YH et al., Cancers (Basel) 2023 (PMID:36672499)
Liao WL et al., Int J Mol Sci 2022 (PMID:36613808)
Ya-Hui Chen et al., Cancers (Basel) 2022 (PMID:35406599)
Yang YS et al., Oncotarget 2016 (PMID:27050378)
Chia-Hung Yeh et al., Materials 2015;8(7)
Chiang WF et al., Oral Oncol 2013 (PMID:23375593)
Quantification of Myocyte Chemotaxis: A Role for FAK in Regulating Directional Motility
in motility and a single-cell tracking assay to identify signals that drive the coordinated movement of these cells. These methods have proven effective to identify focal adhesion kinase (FAK) as an intracellular component that is critical for myocyte
Inflammation and Tumor Progression: A Lesson from TNF--Dependent FAK Signaling in Cholangiocarcinoma
Focal Adhesion Kinase (FAK) is implicated in a wide array of cellular processes and also involved in the production of matrix metalloproteinases (MMPs) which degrade extracellular matrix (ECM). We have shown that FAK plays a critical role
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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