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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. Suitable for WB, IHC(P), and ICC/IF applications. Affinity-purified with >95% purity. Supplied as a liquid, 1 mg/mL concentration. Store at 4°C short term or -20°C long term.

카탈로그번호
PA577109
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 03:41
Thermo Fisher Scientific PA577109 NMT2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
799,300원VAT 포함 879,230원

Thermo Fisher Scientific · Thermo Fisher Scientific NMT2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200

Product Specifications

Specification Description
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full-length Human NMT2 (amino acids 1–498)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
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_2720836

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Proteolytic degradation is essential for 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 cytosolic and nuclear proteins in eukaryotic cells, while others are degraded via the vacuolar pathway involving endosomes, lysosomes, and the endoplasmic reticulum.
The 26S proteasome is an ATP-dependent, multisubunit complex (~2.5 MDa) composed of a 20S proteolytic core and 19S regulatory subunits that recognize ubiquitinated proteins, unfold them, and translocate them into the 20S core for degradation.
Defects in this pathway are associated with several genetic diseases, including cystic fibrosis, Angelman syndrome, and Liddle syndrome.


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

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