- ￥5600
- GeneTex
- 美国
- GTX31879
- 2025年07月12日
- WB, IHC-P, ELISA
- Rabbit
- Human, Mouse, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
TORC2 antibody was raised against a 16 amino acid peptide near the carboxy terminus of human TORC2 .The immunogen is located within the last 50 amino acids of TORC2 .
- 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：
GTX31879
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, IHC-P, ELISA
- 浓度：
1 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
Multiple isoforms are known to exist.This antibody is predicted to not cross-react with CRTC1.
- 抗体英文名：
TORC2 antibody
- 抗体名：
TORC2 抗体
- 规格：
100 μg
IHC-P analysis of human small intestine tissue using GTX31879 TORC2 antibody.
Working concentration : 20 μg/ml
WB analysis of human small intestine tissue lysate using GTX31879 TORC2 antibody.
Working concentration : (A) 0.5 and (B) 1 μg/ml
IHC-P analysis of human small intestine tissue using GTX31879 TORC2 antibody.
Working concentration : 2.5 μg/ml
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文献和实验Lee MY et al., Int J Mol Sci 2019 (PMID:31540136)
at the leading edge of the cell, has been extensively characterized. However, chemotaxis still remains in cells depleted of PIP3 , suggesting there are PIP3 -independent pathways. We have identified a pathway involving TorC2-PKBR1 as well as another containing
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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