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

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Rabbit polyclonal antibody against human NMT2. Validated for WB and IP applications. Supplied as a liquid at 1 mg/mL concentration. Recommended storage at 4°C. For research use only.

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pk
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마지막 업데이트 2025. 08. 03. 오전 05:51
Thermo Fisher Scientific A304359AM NMT2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
477,300원VAT 포함 525,030원
Thermo Fisher Scientific A304359AT NMT2 Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific NMT2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:2,000–1:10,000
Immunoprecipitation (IP) Assay-dependent

Product Specifications

Specification Description
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 100 to 150 of human N-myristoyltransferase 2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • Based on 100% sequence identity, this antibody is predicted to react with Bovine

Target Information

Proteolytic degradation is critical to maintaining appropriate levels of short-lived and regulatory proteins involved in cellular metabolism, stress response, antigen presentation, modulation of cell surface receptors and ion channels, cell cycle regulation, transcription, and signaling.
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) molecular complex (~2.5 MDa) composed of a 20S proteolytic core and 19S regulatory subunits. These subunits recognize ubiquitinated proteins and facilitate their unfolding and translocation into the 20S core.
An enzymatic cascade attaches multiple ubiquitin molecules to lysine residues of target proteins for degradation.
Defects in the ubiquitin-proteasome 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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