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

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Rat NOTCH2 단백질을 인식하는 Goat Polyclonal Antibody로, Western Blot, IHC, Flow Cytometry 등에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS와 trehalose buffer에 보존. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 03. 오전 09:44
Thermo Fisher Scientific PA547091 NOTCH2 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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704,800원VAT 포함 775,280원

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) 0.1 µg/mL -
Immunohistochemistry (IHC) - View 1 publication
Immunohistochemistry (Frozen) (IHC (F)) 5–15 µg/mL -
Flow Cytometry (Flow) 2.5 µg per million cells -
Neutralization (Neu) Assay-Dependent -

Product Specifications

Specification Detail
Species Reactivity Rat
Published Species Rat
Host / Isotype Goat / IgG
Class Polyclonal
Type Antibody
Immunogen Mouse myeloma cell line NS0-derived recombinant rat Notch-2 (Leu26–Glu492)
Conjugate Unconjugated
Form Lyophilized
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 5% trehalose
Contains No Preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2576813

Product Specific Information

  • In direct ELISAs and Western blots, approximately 5% cross-reactivity with recombinant rat Notch-1 is observed, and less than 1% cross-reactivity with recombinant mouse Notch-3.
  • Reconstitute at 0.2 mg/mL in sterile PBS.
  • Endotoxin level: <0.10 EU per 1 µg of antibody (LAL method).

Target Information

Neurogenic locus notch homolog protein 2 (NOTCH2) is a highly conserved Notch signaling pathway protein.
NOTCH2 is a type 1 transmembrane protein with an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain with diverse domain types.
It functions as a receptor for membrane-bound ligands 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.
Facial features are characteristic, with occasional renal and vascular system involvement.


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

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