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ELK Biotechnology c-Abl (phospho-Tyr89)  rabbit pAb
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ELK Biotechnology c-Abl (phospho-Tyr89) rabbit pAb

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c-Abl (phospho-Tyr89) rabbit polyclonal antibody로, 인산화된 Tyr89 부위를 특이적으로 인식합니다. Western blot에 적합하며, 사람, 쥐, 생쥐 시료에서 반응합니다. 세포 내 신호전달 및 암 관련 연구에 유용합니다.

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pk
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ELK Biotechnology ES17895-100UL c-Abl (phospho-Tyr89) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES17895-50UL c-Abl (phospho-Tyr89) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology c-Abl (phospho-Tyr89) rabbit pAb

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c-Abl (phospho-Tyr89) rabbit pAb

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항목 내용
Product name c-Abl (phospho-Tyr89) rabbit pAb
Alternative Names Tyrosine-protein kinase ABL1 (EC 2.7.10.2), Abelson murine leukemia viral oncogene homolog 1, Abelson tyrosine-protein kinase 1, Proto-oncogene c-Abl, p150
Applications WB
Recommended Dilutions WB 1:1000–2000
Immunogen Synthesized phospho peptide around human c-Abl (Tyr89)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 140 kDa (200 kDa BCR-ABL complex)
GeneID (Human) 25
Human Swiss-Prot No P00519
Cellular Localization Cytoplasm, cytoskeleton, nucleus, mitochondrion. Shuttles between nucleus and cytoplasm depending on environmental signals. Sequestered into cytoplasm via interaction with 14-3-3 proteins. Localizes to mitochondria in response to oxidative stress. Isoform IB: nucleus membrane, lipid-anchor. Myristoylated c-ABL protein is reported to be nuclear.
Species Reactivity Human, Rat, Mouse

Background

This gene is a proto-oncogene that encodes a protein tyrosine kinase involved in cellular processes such as cell division, adhesion, differentiation, and stress response. The protein’s activity is negatively regulated by its SH3 domain; deletion of this region results in oncogenic transformation. It possesses DNA-binding activity regulated by CDC2-mediated phosphorylation, suggesting a role in the cell cycle. The gene is known to form fusions with various translocation partners in leukemias, most notably the t(9;22) translocation producing the BCR-ABL fusion. Alternative splicing yields two transcript variants with alternative first exons joined to common exons.

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