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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI7C9), TrueMAB
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Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI7C9), TrueMAB

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UFD1L 단백질을 인식하는 Mouse monoclonal antibody로 Western blot과 IHC(Paraffin)에 적합합니다. E.coli에서 생산된 full-length human recombinant protein을 면역원으로 사용하였으며, carrier-free 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 04. 오전 07:20
Thermo Fisher Scientific CF804319 UFD1L Monoclonal Antibody (OTI7C9), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI7C9), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone OTI7C9
Immunogen Full length human recombinant protein of human UFD1L produced in E.coli
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using the carrier-free antibody, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

Ubiquitin-mediated proteolysis involves the transfer of ubiquitin (Ub) to lysine residues on specific cellular proteins, leading to their degradation by the 26S proteasome. Ub-fusions are cleaved by Ub-specific proteases (UBps) or through the Ub-fusion degradation (UFD) pathway.
UFD proteins preferentially cleave Ub-conjugated proteins with an amino acid substitution at the C-terminal glycine residue of Ub. The UFD1 protein, first identified in yeast (S. cerevisiae), has a human homolog known as UFD1L. In vitro, UFD1 attenuates degradation of Ub-fusions containing a proline or valine substitution at Gly76 by promoting selective multiubiquitination.
Mutations in the UFD1 gene are associated with CATCH22 syndrome, which includes cardiac defects, cleft palate, and hypocalcemia, suggesting a role for this pathway in developmental processes.


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

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