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Thermo Fisher Scientific PSME1 Recombinant Rabbit Monoclonal Antibody (29D5)
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Thermo Fisher Scientific PSME1 Recombinant Rabbit Monoclonal Antibody (29D5)

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PSME1 단백질을 인식하는 Thermo Fisher의 재조합 토끼 단일클론 항체로, Western blot, IHC, ICC, Flow cytometry, ELISA 등 다양한 응용에 적합합니다. 인간 시료 반응성이 있으며, HEK293 세포 발현 시스템에서 생산된 고순도 항체입니다.

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마지막 업데이트 2025. 08. 05. 오전 03:42
Thermo Fisher Scientific MA550005 PSME1 Recombinant Rabbit Monoclonal Antibody (29D5) 100 ul pk판매 단위 pk ·
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643,200원VAT 포함 707,520원

Thermo Fisher Scientific · Thermo Fisher Scientific PSME1 Recombinant Rabbit Monoclonal Antibody (29D5)

Applications and Tested Dilution

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
Flow Cytometry (Flow) 1:50–1:200
ELISA Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 29D5
Immunogen A synthesized peptide derived from human PSME1
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C or -80°C if preferred
Shipping Conditions Wet ice
RRID AB_3092496

Target Information

Proteolytic degradation is critical for maintaining appropriate levels of short-lived and regulatory proteins involved in cellular metabolism, stress response, antigen presentation, receptor modulation, ion channels, 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 (approx. 31), barrel-shaped 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 assist in unfolding and translocating them into the 20S lumen.

An enzymatic cascade attaches multiple ubiquitin molecules to lysine residues of target proteins for degradation. Defects in this pathway are associated with 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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