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Thermo Fisher Scientific SHP2 Polyclonal Antibody
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Thermo Fisher Scientific SHP2 Polyclonal Antibody

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SHP2 단백질을 인식하는 Thermo Fisher Scientific의 다클론성 항체로, WB, ICC/IF, Flow Cytometry에 사용 가능. Human, Mouse, Rat 반응성. Rabbit IgG 기반, Lyophilized 형태. 세포 신호 조절 연구 및 Noonan 증후군 관련 연구에 적합.

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pk
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마지막 업데이트 2025. 08. 01. 오후 08:22
Thermo Fisher Scientific PA595069 SHP2 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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618,800원VAT 포함 680,680원

Thermo Fisher Scientific · Thermo Fisher Scientific SHP2 Polyclonal Antibody

Thermo Fisher Scientific SHP2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 0.1–0.5 µg/mL View 1 publication
Immunocytochemistry (ICC/IF) 5 µg/mL -
Flow Cytometry (Flow) 1–3 µg/1×10⁶ cells -

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide corresponding to a sequence at the C-terminus of human SHP2 (582–597aa RVYENVGLMQQQKSFR).
Conjugate Unconjugated
Form Lyophilized
Concentration 500 µg/mL
Purification Affinity chromatography
Storage Buffer PBS with 4 mg trehalose
Contains No preservative
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_2806875

Product Specific Information

Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.


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, which function as phospho-tyrosine binding domains and mediate interactions with substrates.
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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