
ELK Biotechnology Abl1 (phospho Thr735) rabbit pAb
ABL1 단백질의 Thr735 인산화 부위를 인식하는 rabbit polyclonal 항체. WB, IHC, IF, ELISA에 적합하며, 세포 내 신호전달 및 종양 연구에 활용 가능. 인간, 마우스, 랫드, 원숭이에 반응. -20°C에서 1년 보관.
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제품명
Abl1 (phospho Thr735) rabbit pAb
대체 명칭
ABL1; ABL; JTK7; Tyrosine-protein kinase ABL1; Abelson murine leukemia viral oncogene homolog 1; Abelson tyrosine-protein kinase 1; Proto-oncogene c-Abl; p150
적용 분야 (Applications)
- WB (Western Blot)
- IHC (Immunohistochemistry)
- IF (Immunofluorescence)
- ELISA
권장 희석 배수 (Recommended Dilutions)
- Western Blot: 1/500 - 1/2000
- Immunohistochemistry: 1/100 - 1/300
- ELISA: 1/5000
- Other applications: Not yet tested
면역원 (Immunogen)
The antiserum was produced against a synthesized peptide derived from human ABL1 around the phosphorylation site of Thr735.
Amino acid range: 701–750
제품 사양 (Specifications)
| 항목 | 내용 |
|---|---|
| Host | Rabbit |
| Storage | -20°C / 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | 125 kDa (200 kDa BCR-ABL complex) |
| Gene ID (Human) | 25 |
| Human Swiss-Prot No. | P00519 |
| Species Reactivity | Human, Mouse, Rat, Monkey |
세포 내 위치 (Cellular Localization)
Cytoplasm, cytoskeleton, nucleus, and mitochondrion.
Shuttles between the nucleus and cytoplasm depending on environmental signals.
Sequestered into the cytoplasm through interaction with 14-3-3 proteins.
Localizes to mitochondria in response to oxidative stress.
Isoform IB: nucleus membrane, lipid-anchor. The myristoylated c-ABL protein is reported to be nuclear.
배경 (Background)
This gene is a proto-oncogene encoding a protein tyrosine kinase involved in various cellular processes such as cell division, adhesion, differentiation, and stress response.
Its activity is negatively regulated by the SH3 domain; deletion of this domain can result in oncogenic transformation.
The protein exhibits DNA-binding activity regulated by CDC2-mediated phosphorylation, suggesting a role in the cell cycle.
ABL1 is often fused with partner genes in leukemias, most notably in the t(9;22) translocation forming the BCR-ABL fusion gene.
Alternative splicing results in two transcript variants with different first exons spliced to common downstream exons.
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