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Thermo Fisher Scientific SHP2 Monoclonal Antibody (6D9)
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Thermo Fisher Scientific SHP2 Monoclonal Antibody (6D9)

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Human SHP2(PTPN11) 단백질을 인식하는 Mouse monoclonal antibody(6D9)로, WB, IHC, ICC, Flow, ELISA에 사용 가능. Protein G 정제, 1 mg/mL 농도, PBS buffer에 0.05% sodium azide 포함. 단기 4°C, 장기 -20°C 보관 권장.

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마지막 업데이트 2025. 08. 05. 오후 04:21
Thermo Fisher Scientific MA517160 SHP2 Monoclonal Antibody (6D9) 100 ug pk판매 단위 pk ·
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661,800원VAT 포함 727,980원

Thermo Fisher Scientific · Thermo Fisher Scientific SHP2 Monoclonal Antibody (6D9)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:1,000
Immunocytochemistry (ICC/IF) 1:200–1:1,000
Flow Cytometry (Flow) 1:200–1:400
ELISA 1:10,000

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 6D9
Immunogen Purified recombinant fragment of human PTPN11 (amino acids 263–329) expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2538631

Product Specific Information

MA5-17160 targets PTPN11 in indirect ELISA, FACS, ICC, IHC, IF, and WB applications, showing reactivity with human samples.
The immunogen is a purified recombinant fragment of human PTPN11 (amino acids 263–329) expressed in E. coli.
MA5-17160 detects PTPN11, which has a predicted molecular weight of approximately 68.4 kDa.

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, functioning as phospho-tyrosine binding domains mediating substrate interactions. It is widely expressed in most tissues and plays a regulatory role in cell signaling events 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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