- 询价
- Cell Signaling Technology
- 6929
- USA
- 2025年12月09日
- W
- Rabbit
- M,R
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- 详细信息
- 文献和实验
- 技术资料
- 抗体英文名：
Phospho-TBC1D1 (Ser700) Antibody
- 抗原：
synthetic peptide corresponding to residues surrounding Ser700 of mouse TBC1D1 protein
- 应用范围：
W
- 宿主：
Rabbit
- 级别：
详见MSDS文件
- 库存：
大量
- 保质期：
详见说明书
- 供应商：
CST
- 适应物种：
M,R
- 是否单克隆：
2
- 保存条件：
-20°c
- 规格：
100 ul (10 western blots)/carrier free & custom formulation / quantity
| 规格： | 产品价格： | ￥请询价 | |
|---|---|---|---|
| 规格： | 100 ul (10 western blots) | 产品价格： | ￥请询价 |
| 规格： | carrier free & custom formulation / quantity | 产品价格： | ￥请询价 |
pathway more info application references datasheet PDF MSDS PDF protocols
Applications Key: W=Western Blotting
Reactivity Key: M=Mouse R=Rat
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
| Applications | Reactivity | Sensitivity | MW (kDa) | Source |
|---|---|---|---|---|
| W | M (R) | Transfected Only | 160 | Rabbit |
| Protocols |
|
|---|---|
| Specificity / Sensitivity | Phospho-TBC1D1 (Ser700) Antibody detects transfected levels of TBC1D1 protein when phosphorylated at Ser700. |
| Source / Purification | Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ser700 of mouse TBC1D1 protein. Antibodies are purified by protein A and peptide affinity chromatography. Western Blotting
Western blot analysis of extracts from 293T cells, untransfected or transfected with mouse wild-type TBC1D1 or mutant TBC1D1 (S700A), using Phospho-TBC1D1 (Ser700) Antibody (upper panel) or TBC1D1 (G689) Antibody #5929 (lower panel). Both of the above expression vectors were kindly provided by Dr. Laurie Goodyear at the Joslin Diabetes Center. |
| Background | TBC1D1 is a paralog of AS160 (1) and both proteins share about 50% identity (2). TBC1D1 was shown to be a candidate gene for severe obesity (3). It plays a role in Glut4 translocation through its GAP activity (2,4). Studies indicate that TBC1D1 is highly expressed in skeletal muscle (1). Insulin, AICAR, and contraction directly regulate TBC1D1 phosphorylation in this tissue (1). Three AMPK phosphorylation sites (Ser231, Ser660, and Ser700) and one Akt phosphorylation site (Thr590) were identified (5). Muscle contraction or AICAR treatment increases phosphorylation on Ser231, Ser660, and Ser700 but not on Thr590; insulin increases phosphorylation on Thr590 only (5). |
| Application References | Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know ! |
| Companion Products |
For Research Use Only. Not For Use In Diagnostic Procedures. |
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文献和实验Using Phospho‐Motif Antibodies to Determine Kinase Substrates
comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available
Optimized Protocol to Make Phospho-Specific Antibodies that Work
, not simply its level of expression. In this review, we will discuss both the design of the phosphopeptide immunogen and immunization. The affinity purification of the phospho-specific antibody as well as the methods most suitable for characterizing
Absorption Control in Immunohistochemistry Using Phospho-Peptides Immobilized on Magnetic Beads
neutralization of phospho-specific antibodies with phospho-peptides immobilized on magnetic beads. This technique allows for sequestration of antibody–peptide complex from the incubation solution, minimizing the risk of formation of unblocked antibodies capable
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