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Thermo Fisher Scientific PTPN11 Monoclonal Antibody (OTI2F4), TrueMAB
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Thermo Fisher Scientific PTPN11 Monoclonal Antibody (OTI2F4), TrueMAB

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PTPN11 단백질을 인식하는 마우스 단클론 항체로, Western blot과 유세포분석에 적합합니다. HEK293T 세포에서 생산된 재조합 단백질을 면역원으로 사용하며, 고순도의 친화 크로마토그래피 정제 제품입니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 04. 오전 09:36
Thermo Fisher Scientific CF501759 PTPN11 Monoclonal Antibody (OTI2F4), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific PTPN11 Monoclonal Antibody (OTI2F4), TrueMAB

Applications

Western Blot (WB)

  • Tested Dilution: 1:1,000

Flow Cytometry (Flow)

  • Tested Dilution: 1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI2F4
Immunogen Full length human recombinant protein of human PTPN11 produced in HEK293T cell
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, we recommend adding 100 µL distilled water to achieve a final antibody concentration of about 1 mg/mL.
To use this carrier-free antibody for conjugation experiments, we strongly recommend performing another round of desalting.
(Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882)

Target Information

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are 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 function as phospho-tyrosine binding domains and mediate substrate interactions.
It is widely expressed in most tissues and plays a regulatory role in cell signaling events important for 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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