
Thermo Fisher Scientific UFD1L Monoclonal Antibody (OTI7C9), TrueMAB
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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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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