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

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NOTCH2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 ChIP-Seq에 사용 가능. 인간 및 마우스 반응성. 고순도 항원 친화 크로마토그래피로 정제된 액상 항체. 연구용으로만 사용.

카탈로그번호
PA527458
판매단위
pk
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마지막 업데이트 2025. 07. 31. 오전 01:14
Thermo Fisher Scientific PA527458 NOTCH2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

Thermo Fisher Scientific · Thermo Fisher Scientific NOTCH2 Polyclonal Antibody

Thermo Fisher Scientific NOTCH2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:3,000 -
ChIP-sequencing (ChIP-Seq) Assay-dependent -

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to a region within amino acids 1669–1855 of Human NOTCH2
Conjugate Unconjugated
Form Liquid
Concentration 0.43 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 1% BSA, 20% glycerol
Contains 0.025% ProClin 300
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2544934

Product Specific Information

  • Recommended positive controls: A431, HeLa, HepG2
  • Predicted reactivity: Mouse (95%), Rat (89%), Rhesus Monkey (99%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Neurogenic locus notch homolog protein 2 (NOTCH2) is a highly conserved Notch signaling pathway protein. NOTCH2 is a type I transmembrane protein with an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple, distinct domain types.
NOTCH2 functions as a receptor for membrane-bound ligands Jagged1, Jagged2, and Delta1 to regulate cell-fate determination.
Defects in NOTCH2 are the cause of Alagille syndrome type 2 (ALGS2), an autosomal dominant multisystem disorder characterized by hepatic bile duct paucity and cholestasis, along with cardiac, skeletal, and ophthalmologic manifestations.

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

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