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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3E9), TrueMAB
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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3E9), TrueMAB

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인간 UFD1L 단백질을 인식하는 단클론 항체로, Western blot에 최적화되어 있음. TrueMAB 포맷으로 높은 특이성과 재현성을 제공. 액상 형태로 1 mg/mL 농도, PBS/BSA/glycerol 완충액에 보관. 연구용으로만 사용 가능.

카탈로그번호
TA804288
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:11
Thermo Fisher Scientific TA804288 UFD1L Monoclonal Antibody (OTI3E9), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3E9), TrueMAB

Applications

  • Western Blot (WB): Tested at 1:2,000 dilution

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI3E9
Immunogen Full length human recombinant protein of human UFD1L produced in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 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

Ubiquitin-mediated proteolysis requires the transfer of ubiquitin (Ub) to lysine groups on selected cellular proteins, which then potentiates the proteolytic degradation of these protein conjugates by the 26S proteasome. Ub-fusions are cleaved by Ub-specific processing proteases (UBps) or alternatively by the Ub-fusion degradation (UFD) pathway.
The UBP pathway targets the C-terminal glycine residue on Ub involved in the formation of Ub-conjugates, while UFD proteins preferentially cleave Ub-conjugated proteins that contain an amino acid substitution at this glycine residue.
The UFD1 protein was originally characterized in S. cerevisiae and subsequently, the human homolog UFD1 or UFD1L was identified. In vitro, UFD1 attenuates degradation of Ub-fusions with proline or valine substitution at the Gly76 moiety by selective multiubiquitination of the Ub chain.
Mutations within the UFD1 gene are implicated in CATCH22 syndrome, characterized by cardiac defects, cleft palate, and hypocalcemia, suggesting involvement of this proteolytic pathway in developmental defects.

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

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