
ELK Biotechnology Trk A (phospho Tyr701) rabbit pAb
Trk A (phospho Tyr701) rabbit polyclonal antibody로, 인간·마우스·랫트 시료에 반응합니다. WB, IHC, IF, ELISA 등 다양한 응용에 적합하며, Tyr701 인산화 부위를 인식합니다. 세포막 및 엔도솜에 위치한 단백질 검출에 유용합니다.
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제품명
Trk A (phospho Tyr701) rabbit pAb
제품 개요
본 항체는 인간 Trk A 단백질의 Tyr701 인산화 부위를 기반으로 제작된 rabbit polyclonal antibody입니다. 다양한 응용(WB, IHC, IF, ELISA)에 적합하며, 세포막 및 엔도솜에 위치한 Trk A 단백질의 검출에 활용됩니다.
제품 정보
| 항목 | 내용 |
|---|---|
| Product Name | Trk A (phospho Tyr701) rabbit pAb |
| Alternative Names | NTRK1; MTC; TRK; TRKA; High affinity nerve growth factor receptor; Neurotrophic tyrosine kinase receptor type 1; TRK1-transforming tyrosine kinase protein; Tropomyosin-related kinase A; Tyrosine kinase receptor; Tyrosine kinase receptor A |
| Applications | WB; IHC; IF; ELISA |
| Recommended Dilutions | WB: 1/500–1/2000 IHC: 1/100–1/300 ELISA: 1/40000 Not yet tested in other applications |
| Immunogen | Synthesized peptide derived from human Trk A around phosphorylation site of Tyr701 (AA range: 666–715) |
| Host | Rabbit |
| Storage | -20°C / 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | 140–180 kDa |
| Gene ID (Human) | 4914 |
| Human Swiss-Prot No. | P04629 |
| Species Reactivity | Human; Mouse; Rat |
세포 내 위치
Cell membrane; Single-pass type I membrane protein.
Early endosome membrane; Single-pass type I membrane protein.
Late endosome membrane; Single-pass type I membrane protein.
Recycling endosome membrane; Single-pass type I membrane protein.
Rapidly internalized after NGF binding (PubMed:1281417).
Internalized to endosomes upon NGF or NTF3 binding and transported to the cell body via retrograde axonal transport.
Localized at cell membrane and early endosomes before NGF stimulation; recruited to late endosomes after NGF stimulation; colocalized with RAPGEF2 at late endosomes.
Background
This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, mental retardation, and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date. [provided by RefSeq, Jul 2008]
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