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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 토끼 유래 다클론 항체입니다. Western blot, IHC, ICC/IF에 적합하며, 고순도의 항원 친화 크로마토그래피로 정제되었습니다. 단기 4°C, 장기 -20°C 보관 권장.

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마지막 업데이트 2025. 08. 03. 오후 01:29
Thermo Fisher Scientific PA531114 UFD1L Polyclonal Antibody 100 ul pk판매 단위 pk ·
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660,800원VAT 포함 726,880원

Thermo Fisher Scientific · Thermo Fisher Scientific UFD1L Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to a region within amino acids 45–307 of Human UFD1L
Conjugate Unconjugated
Form Liquid
Concentration 0.66 mg/mL
Purification Antigen affinity chromatography
Storage Buffer 0.1M Tris glycine, pH 7, with 20% glycerol
Contains 0.01% thimerosal
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_2548588

Product Specific Information

  • Recommended positive control: A431
  • Predicted reactivity: Mouse (98%), Rat (97%), Zebrafish (84%), Xenopus laevis (88%), Chicken (92%), Rhesus Monkey (99%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

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.


WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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