Cell Signaling Technology

Product Pathways - Neuroscience

Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8) Rabbit mAb #4168


No. Size Price
4168S 100 µl ( 10 western blots ) ¥4,050.00 现货查询 购买询价 防伪查询
4168T 20 µl ( 2 western blots ) ¥1,500.00 现货查询 购买询价 防伪查询
4168 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Rat, Endogenous 140 Rabbit IgG

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting,


Species predicted to react based on 100% sequence homology: Human, Mouse,

Specificity / Sensitivity

Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8) Rabbit mAb detects endogenous levels of TrkA and TrkB when phosphorylated at Tyr785 of TrkA or Tyr816 of TrkB. This antibody may cross-react with other tyrosine-phosphorylated proteins.

Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8)Rabbit mAb兔单抗可识别内源性的Tyr785/Tyr816磷酸化的TrkA/TrkB。此抗体与其它酪氨酸磷酸化蛋白没有交叉反应。

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr785 of human TrkA protein.


Western Blotting

Western Blotting

Western blot analysis of extracts from NIH/3T3 cells transfected with TrkA, untreated or treated with NGF, using Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8) Rabbit mAb (upper) and TrkA (14G6) Rabbit mAb #2508 (lower).

Western blot分析转染了TrkB的NIH/3T3细胞,未处理或使用NGF处理,使用的抗体是Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8)Rabbit mAb兔单抗(上图)和TrkA (14G6)Rabbit mAb 兔单抗#2508(下图)进行。

Western Blotting

Western Blotting

Western blot analysis of extracts from NIH/3T3 cells transfected with TrkB, untreated or treated with hBDNF #3897, using Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8) Rabbit mAb (upper) and Trk (pan) (C17F1) Rabbit mAb #4609 (lower).

Western blot分析转染了TrkB的NIH/3T3细胞,未处理或使用hBDNF #3897预处理,然后使用Phospho-TrkA (Tyr785)/TrkB (Tyr816) (C67C8) Rabbit mAb 兔单抗(上图)和Trk (pan) (C17F1) Rabbit mAb 兔单抗#4609(下图)。


The family of Trk receptor tyrosine kinases consists of TrkA, TrkB and TrkC. While the sequence of these family members is highly conserved, they are activated by different neurotrophins: TrkA by NGF, TrkB by BDNF or NT4, and TrkC by NT3. TrkA regulates proliferation and is important for development and maturation of the nervous system (1). Phosphorylation at Tyr490 is required for Shc association and activation of the Ras-MAP kinase cascade. Residues Tyr674/675 lie within the catalytic domain, and phosphorylation at this site reflects TrkA kinase activity (2-6). Point mutations, deletions and chromosomal rearrangements (chimeras) cause ligand-independent receptor dimerization and activation of TrkA. Many malignancies including breast, colon, prostate and thyroid carcinomas and acute myeloid leukemia have activated TrkA. Expression of TrkA in neuroblastomas is a good prognostic marker because it signals growth arrest and differentiation of cells originating from the neural crest (1).Phosphorylation at Tyr785 is required for activation of phospholipase Cγ and subsequent activation of the Ras-MAP kinase cascade. The phosphorylation site is conserved between TrkA and TrkB, as Tyr785 of TrkA corresponds to Tyr816 in TrkB of the human sequence (4,7).


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  12. Greco, A. et al. (2010) Mol Cell Endocrinol 321, 44-9.
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  14. Chou, T.T. et al. (2000) J Biol Chem 275, 565-70.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

U.S. Patent No. 5,675,063.

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