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Thermo Fisher Scientific NMT2 Monoclonal Antibody (OTI1G3), TrueMAB
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Thermo Fisher Scientific NMT2 Monoclonal Antibody (OTI1G3), TrueMAB

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인간 NMT2 단백질을 인식하는 Mouse IgG1 단일클론 항체로 Western blot 및 IHC(P) 분석에 적합. 고순도 친화 크로마토그래피 정제, 액상 형태로 제공되며 안정적인 PBS/BSA/glycerol 버퍼에 보존. 연구용 단백질 발현 및 분해 연구에 활용 가능.

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TA504158
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 06:41
Thermo Fisher Scientific TA504158 NMT2 Monoclonal Antibody (OTI1G3), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific NMT2 Monoclonal Antibody (OTI1G3), TrueMAB

Thermo Fisher Scientific NMT2 Monoclonal Antibody (OTI1G3), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC(P)) 1:150

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI1G3
Immunogen Full length human recombinant protein of human NMT2 produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 0.69 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

Proteolytic degradation is critical to maintaining appropriate levels of short-lived and regulatory proteins involved in cellular metabolism, heat shock and stress response, antigen presentation, modulation of cell surface receptors and ion channels, cell cycle regulation, transcription, and signaling factors.
The ubiquitin-proteasome pathway deconstructs most proteins in the eukaryotic cell cytosol and nucleus, while others are degraded via the vacuolar pathway involving endosomes, lysosomes, and the endoplasmic reticulum.
The 26S proteasome is an ATP-dependent, multisubunit (~31), barrel-shaped molecular machine (~2.5 MDa) composed of a 20S proteolytic core complex with 19S regulatory subunits. These recognize ubiquitinated proteins and facilitate unfolding and translocation into the 20S lumen.
Defects in this pathway are associated with genetic diseases such as cystic fibrosis, Angelman’s syndrome, and Liddle syndrome.

Usage Note

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

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