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Thermo Fisher Scientific NMT2 Polyclonal Antibody
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Thermo Fisher Scientific NMT2 Polyclonal Antibody

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Thermo Fisher Scientific의 NMT2 Polyclonal Antibody는 인간, 마우스, 랫트 반응성을 가지며 다양한 면역 분석(WB, IHC, ICC, ELISA)에 사용 가능합니다. KLH 결합 합성 펩타이드로부터 제작된 Rabbit IgG 항체로, 고순도 Protein A 정제 및 안정적 액상 형태로 제공됩니다.

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마지막 업데이트 2025. 07. 21. 오전 05:31
Thermo Fisher Scientific BS-6233R NMT2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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531,800원VAT 포함 584,980원

Thermo Fisher Scientific · Thermo Fisher Scientific NMT2 Polyclonal Antibody

Thermo Fisher Scientific NMT2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:300–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (Frozen) (IHC (F)) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide derived from human NMT2, amino acids 201–300
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA
Contains 0.02% ProClin 300
Storage Conditions -20°C
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, stress response, antigen presentation, receptor modulation, cell cycle regulation, transcription, and signaling.
The ubiquitin-proteasome pathway deconstructs most proteins in the eukaryotic 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 and 19S regulatory subunits. The 19S complexes recognize ubiquitinated proteins and facilitate unfolding and translocation into the 20S lumen.
Defects in this pathway are linked to genetic diseases such as cystic fibrosis, Angelman’s syndrome, and Liddle syndrome.

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

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