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Thermo Fisher Scientific Phospho-Shp2 (Tyr580) Recombinant Rabbit Monoclonal Antibody (Shp2Y580-4A2), APC
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Thermo Fisher Scientific Phospho-Shp2 (Tyr580) Recombinant Rabbit Monoclonal Antibody (Shp2Y580-4A2), APC

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APC 형광 표지된 Recombinant Rabbit Monoclonal 항체로 Tyr580 위치의 인산화 Shp2 단백질을 특이적으로 인식합니다. 인간 및 생쥐 시료에 반응하며 Flow Cytometry에 적합합니다. 고순도 Protein A/G 정제, PBS+BSA buffer로 안정적 보관 가능.

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마지막 업데이트 2025. 08. 04. 오전 05:15
Thermo Fisher Scientific MA536980 Phospho-Shp2 (Tyr580) Recombinant Rabbit Monoclonal Antibody (Shp2Y580-4A2), APC 100 tests pk판매 단위 pk ·
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700,900원VAT 포함 770,990원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-Shp2 (Tyr580) Recombinant Rabbit Monoclonal Antibody (Shp2Y580-4A2), APC

Thermo Fisher Scientific Phospho-Shp2 (Tyr580) Recombinant Rabbit Monoclonal Antibody (Shp2Y580-4A2), APC

Applications

  • Flow Cytometry (Flow)

Tested Dilution: 5 µL / 1×10⁶ cells

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG, kappa
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone Shp2Y580-4A2
Immunogen Synthetic phospho-peptide corresponding to residues surrounding Tyr580 of human phospho Shp2
Conjugate APC
Excitation / Emission Max 651 / 660 nm
Form Liquid
Purification Protein A/G
Storage Buffer PBS with 0.20% BSA
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2896915

Additional Formats

  • Unconjugated: MA5-36977
  • FITC: MA5-36979
  • PE: MA5-36978
  • Custom conjugation available upon request

Target Information

The protein encoded by this gene belongs to the protein tyrosine phosphatase (PTP) family. PTPs act as signaling molecules that regulate various cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation.
This PTP contains two tandem Src homology-2 domains that mediate interactions with phospho-tyrosine substrates. It is widely expressed and plays a regulatory role in cell signaling related to mitogenic activation, metabolic control, transcription regulation, and cell migration.
Mutations in this gene are associated with Noonan syndrome and acute myeloid leukemia.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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