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Thermo Fisher Scientific PSMA1 Monoclonal Antibody (OTI6C4), TrueMAB
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Thermo Fisher Scientific PSMA1 Monoclonal Antibody (OTI6C4), TrueMAB

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인간 PSMA1 단백질을 인식하는 Mouse IgG2a 단일클론 항체. Western blot에 최적화되어 있으며, E.coli에서 발현된 full-length recombinant 단백질을 면역원으로 사용. Affinity chromatography로 정제된 액상 형태로, 연구용 단백질 분해 경로 분석에 적합.

카탈로그번호
TA812761
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오후 11:33
Thermo Fisher Scientific TA812761 PSMA1 Monoclonal Antibody (OTI6C4), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific PSMA1 Monoclonal Antibody (OTI6C4), TrueMAB

Applications

  • Western Blot (WB): Tested dilution 1:250

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI6C4
Immunogen Full length human recombinant protein of human PSMA1 produced in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 0.5–1 mg/mL
Purification Affinity chromatography
Storage buffer PBS with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
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 diverse cellular processes such as metabolism, stress response, antigen presentation, receptor modulation, cell cycle regulation, and transcription.
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 (approximately 31 subunits), barrel-shaped molecular complex (~2.5 MDa). It consists of a 20S proteolytic core complex capped by one or two 19S regulatory subunits, which recognize ubiquitinated proteins and facilitate their unfolding and translocation into the 20S core.
An enzymatic cascade mediates the attachment of multiple ubiquitin molecules to lysine residues of target proteins.
Defects in the ubiquitin-proteasome pathway are associated with several genetic diseases, including 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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