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Thermo Fisher Scientific SHP2 Recombinant Rabbit Monoclonal Antibody (3Q4U2)
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Thermo Fisher Scientific SHP2 Recombinant Rabbit Monoclonal Antibody (3Q4U2)

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SHP2 단백질을 인식하는 Recombinant Rabbit Monoclonal Antibody (Clone 3Q4U2). Western blot, ICC/IF, ELISA 등 다양한 응용에 적합. 높은 특이성과 재현성을 제공하며, 인체, 생쥐, 랫트 반응성. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오후 02:14
Thermo Fisher Scientific MA535268 SHP2 Recombinant Rabbit Monoclonal Antibody (3Q4U2) 100 ul pk판매 단위 pk ·
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598,300원VAT 포함 658,130원

Thermo Fisher Scientific · Thermo Fisher Scientific SHP2 Recombinant Rabbit Monoclonal Antibody (3Q4U2)

Thermo Fisher Scientific SHP2 Recombinant Rabbit Monoclonal Antibody (3Q4U2)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:1,000–1:2,000
Immunocytochemistry (ICC/IF) 1:200–1:800
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 3Q4U2
Immunogen Synthetic peptide corresponding to amino acids 1–100 of human SHP2 (UniProt ID: Q06124)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C, avoid freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2849170

Product Specific Information

Immunogen sequence:
MTSRRWFHPN ITGVEAENLL LTRGVDGSFL ARPSKSNPGD FTLSVRRNGA VTHIKIQNTG DYYDLYGGEK FATLAELVQY YMEHHGQLKE KNGDVIELKY

Target Information

The SHP2 protein belongs to the protein tyrosine phosphatase (PTP) family, which regulates cellular processes such as growth, differentiation, mitosis, and oncogenic transformation. SHP2 contains tandem Src homology-2 domains that mediate phospho-tyrosine binding and substrate interactions. It is widely expressed across tissues and plays a regulatory role in signaling events related to mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in SHP2 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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