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Thermo Fisher Scientific NOTCH2 Polyclonal Antibody
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Thermo Fisher Scientific NOTCH2 Polyclonal Antibody

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Human 및 Mouse 시료에 반응하는 Rabbit Polyclonal 항체. Western blot, ICC/IF, ELISA에 사용 가능. Affinity Chromatography로 정제된 액상 항체로, PBS/glycerol buffer에 보관. 세포막, 세포질, 핵에서 NOTCH2 단백질 검출에 적합.

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마지막 업데이트 2025. 07. 29. 오후 01:24
Thermo Fisher Scientific PA587455 NOTCH2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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618,800원VAT 포함 680,680원

Thermo Fisher Scientific · Thermo Fisher Scientific NOTCH2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing amino acids 2242–2471 of human NOTCH2 (NP_0777192)
Conjugate Unconjugated
Form Liquid
Concentration 1.16 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2804163

Product Specific Information

Immunogen sequence:
SRLHPVPVPA DWMNRMEVNE TQYNEMFGMV LAPAEGTHPG IAPQSRPPEG KHITTPREPL PPIVTFQLIP KGSIAQPAGA PQPQSTCPPA VAGPLPTMYQ IPEMARLPSV AFPTAMMPQQ DGQVAQTILP AYHPFPASVG KYPTPPSQHS YASSNAAERT PSHSGHLQGE HPYLTPSPES PDQWSSSSPH SASDWSDVTT SPTPGGAGGG QRGPGTHMSE PPHNNMQVYA

Positive Samples: 293T, LO2, HeLa
Cellular Location: Cell membrane, Cytoplasm, Nucleus, Single-pass type I membrane protein

Target Information

Neurogenic locus notch homolog protein 2 (NOTCH2) is a highly conserved protein in the Notch signaling pathway. It is a type I transmembrane receptor with multiple epidermal growth factor-like (EGF) repeats in the extracellular domain and various domains in the intracellular region. NOTCH2 interacts with ligands such as Jagged1, Jagged2, and Delta1 to regulate cell fate determination.
Defects in NOTCH2 cause Alagille syndrome type 2 (ALGS2), an autosomal dominant multisystem disorder characterized by hepatic bile duct paucity, cholestasis, and associated cardiac, skeletal, and ophthalmologic manifestations, sometimes involving renal and vascular systems.


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

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