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Thermo Fisher Scientific Proteasome 20S beta 6 Polyclonal Antibody
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Thermo Fisher Scientific Proteasome 20S beta 6 Polyclonal Antibody

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Proteasome 20S beta 6 단백질을 인식하는 Rabbit Polyclonal 항체. Western blot 및 IHC(P) 실험에 적합하며, Human, Mouse, Rat에 반응. KLH-conjugated synthetic peptide로 면역화. 단백질 분해 및 유비퀴틴-프로테아좀 경로 연구용.

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Thermo Fisher Scientific BS-9358R Proteasome 20S beta 6 Polyclonal Antibody 100 ul pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific Proteasome 20S beta 6 Polyclonal Antibody

Applications and Tested Dilution

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

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide derived from human Proteasome 20S beta 6
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 plays a critical role in maintaining proper levels of short-lived and regulatory proteins involved in processes such as cellular metabolism, stress response, antigen presentation, receptor modulation, cell cycle regulation, and signaling.
The ubiquitin-proteasome pathway is responsible for degrading most cytosolic and nuclear proteins in eukaryotic cells, while other proteins are degraded through 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 one or two 19S regulatory subunits. The 19S subunits recognize ubiquitinated proteins and facilitate their unfolding and translocation into the 20S core. The PA28/11S REG Activator complex, consisting of alpha, beta, and gamma subunits, enhances 20S proteolytic activity.

Defects in the ubiquitin-proteasome pathway are associated with several genetic diseases, including cystic fibrosis (CF transmembrane regulator), Angelman’s syndrome (E6-AP), and Liddle syndrome (endothelial sodium channels).


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

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