
ELK Biotechnology Trk A (phospho Tyr791) rabbit pAb
Trk A (phospho Tyr791) rabbit polyclonal antibody로, 인간, 랫드, 마우스 시료에 반응합니다. IHC, IF, ELISA에 적합하며 고품질 신경성장인자 수용체 인산화 검출에 유용합니다. -20°C에서 1년 보관 가능합니다.
- 판매단위
- pk
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제품명
Trk A (phospho Tyr791) rabbit pAb
제품 정보
| 항목 | 내용 |
|---|---|
| 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 | IHC; IF; ELISA |
| Recommended Dilutions | Immunohistochemistry: 1/100 - 1/300 ELISA: 1/5000 Not yet tested in other applications |
| Immunogen | The antiserum was produced against synthesized peptide derived from human Trk A around the phosphorylation site of Tyr791 (AA range: 747-796) |
| Storage | -20°C / 1 year |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | 140-180 kD |
| Gene ID (Human) | 4914 |
| Human Swiss-Prot No. | P04629 |
| Species Reactivity | Human; Rat; Mouse |
| Cellular Localization | Cell membrane; Single-pass type I membrane protein. Early endosome membrane; Late endosome membrane; Recycling endosome membrane. Rapidly internalized after NGF binding. Internalized to endosomes upon binding of NGF or NTF3 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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