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          • Primary Antibodies ›
          • UFD1L Antibodies

          Fabgennix

          UFD1L Polyclonal Antibody, Biotin

          View all (23) UFD1L antibodies

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          Cite UFD1L Polyclonal Antibody, Biotin

          Additional Information:
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          Product Details

          UFD1L-BIOTIN

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500-1:1,000
          -

          ELISA (ELISA)

          1:10,000
          -

          Immunoprecipitation (IP)

          1:50-1:250
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Purified 20 kDa UFD1L protein

          Conjugate

          Biotin Biotin Biotin

          Form

          Liquid

          Concentration

          0.5-1.5 mg/mL

          Purification

          Affinity chromatography

          Storage buffer

          proprietary buffer, pH 7.4-7.8, with 0.5% BSA, 30% glycerol

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C

          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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          Bioinformatics

          Protein Aliases: UB fusion protein 1; UB fusion protein 1 {ECO:0000250|UniProtKB:Q92890}; ubiquitin fusion degradation 1 like; Ubiquitin fusion degradation protein 1; Ubiquitin fusion degradation protein 1 homolog; ubiquitin fusion degradation protein 1 homolog {ECO:0000250|UniProtKB:Q92890}; ubiquitin like protein; Ubiquitin recognition factor in ER-associated degradation protein 1; UFD1L; ufd1l {ECO:0000312|RGD:619822}; unnamed protein product

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          Gene Aliases: UFD1; UFD1L

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          UniProt ID: (Human) Q92890, (Rat) Q9ES53, (Mouse) P70362

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          Entrez Gene ID: (Human) 7353, (Rat) 84478, (Mouse) 22230

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          Function(s)
          thiol-dependent ubiquitin-specific protease activity protein binding polyubiquitin binding K48-linked polyubiquitin binding receptor binding protein complex binding ATPase binding
          Process(es)
          skeletal system development ubiquitin-dependent protein catabolic process retrograde protein transport, ER to cytosol negative regulation of type I interferon production ERAD pathway negative regulation of RIG-I signaling pathway proteasome-mediated ubiquitin-dependent protein catabolic process cellular response to misfolded protein ER-associated misfolded protein catabolic process
          It has to be done as per old AB suggested Products section.

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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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