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Thermo Fisher Scientific UFD1L Polyclonal Antibody
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Thermo Fisher Scientific UFD1L Polyclonal Antibody

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Thermo Fisher Scientific의 UFD1L Polyclonal Antibody는 인간 UFD1L 단백질을 인식하는 Rabbit IgG 항체로, Western blot 및 IHC(P)에서 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관. 연구용으로만 사용.

카탈로그번호
PA556427
판매단위
pk
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마지막 업데이트 2025. 07. 29. 오전 03:35
Thermo Fisher Scientific PA556427 UFD1L Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific UFD1L Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:20–1:50

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human UFD1L. Recombinant protein control fragment (Product #RP-95339)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2649234

Product Specific Information

Immunogen sequence:
QVESVNLQVA TYSKFQPQSP DFLDITNPKA VLENALRNFA CLTTGDVIAI NYNEKIYELR VMETKPDKAV SIIECDMNVD FDAPLG

Highest antigen sequence identity:

  • Mouse: 100%
  • Rat: 100%

Target Information

Ubiquitin-mediated proteolysis requires the transfer of ubiquitin (Ub) to lysine groups on selected cellular proteins, which then promotes their degradation by the 26S proteasome. Ub-fusions are cleaved by Ub-specific processing proteases (UBps) or by the Ub-fusion degradation (UFD) pathway.
The UFD1 protein, first characterized in yeast S. cerevisiae, has a human homolog known as UFD1L. In vitro, UFD1 attenuates degradation of Ub-fusions containing amino acid substitutions at Gly76 by promoting selective multiubiquitination of the Ub chain.
Mutations in the UFD1 gene are associated with CATCH22 syndrome, characterized by cardiac defects, cleft palate, and hypocalcemia, suggesting a role in developmental processes.


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

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