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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3B4), TrueMAB
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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3B4), TrueMAB

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Human UFD1L 단백질을 인식하는 Mouse IgG1 단일클론 항체로 Western blot에 최적화됨. Affinity chromatography로 정제된 액상형 항체이며, PBS/BSA/glycerol 버퍼에 보존됨. Ubiquitin-mediated proteolysis 연구용으로 적합.

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마지막 업데이트 2025. 08. 04. 오전 02:49
Thermo Fisher Scientific TA804316 UFD1L Monoclonal Antibody (OTI3B4), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI3B4), TrueMAB

Applications

  • Western Blot (WB)

Tested Dilution

  • 1:2,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI3B4
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 that is 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 the yeast S. cerevisiae and subsequently, the human homolog UFD1 or UFD1L was identified. In vitro, UFD1 attenuates the degradation of Ub-fusions, which have a proline or valine residue substituted at the Gly76 moiety, by the selective multiubiquitination of the Ub chain of the Ub-conjugate. Mutations within the UFD1 gene are implicated in the development of CATCH22 syndrome, which is characterized by cardiac defects, cleft palate and hypocalcemia, suggesting that this proteolytic pathway may be involved in the progression of these developmental defects.


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

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