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[KD Validated] Anti-UBE3A Mouse mAb [55K42K03]

Purified Recombinant Mouse Monoclonal Antibody

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货号 规格 价格
M020429
20µL ¥738.00
50µL ¥1380.00
100µL ¥2280.00

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[KD Validated] Anti-UBE3A Mouse mAb [55K42K03]
[KD Validated] Anti-UBE3A Mouse mAb [55K42K03]
[KD Validated] Anti-UBE3A Mouse mAb [55K42K03]
[KD Validated] Anti-UBE3A Mouse mAb [55K42K03]
Product Name[KD Validated] Anti-UBE3A Mouse mAb
DescriptionPurified Recombinant Mouse Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, FC, IF (Cell)/ICC
DilutionWB 1:400~1:2,000; FC 1:200~1:2,000; IF 1:100~1:1,000
ReactivityHuman, Mouse, Rat
HostMouse
ClonalityMonoclonal
Clone No.55K42K03
IsotypeIgG
LabelUnconjugated
ImmunogenRecombinant protein of human UBE3A
FormatAffinity purified monoclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
SynonymsUBE3A; Ubiquitin Protein Ligase E3A; EPVE6AP; HPVE6A; E6-AP; ANCR; AS; Human Papilloma Virus E6-Associated Protein; Human Papillomavirus E6-Associated Protein; Oncogenic Protein-Associated Protein E6-AP; HECT-Type Ubiquitin Transferase E3A; Renal Carcinoma Antigen NY-REN-54; E6AP Ubiquitin-Protein Ligase; Ubiquitin-Protein Ligase E3A; FLJ26981; CTCL Tumor Antigen Se37-2; Angelman Syndrome; EC 2.3.2.26; PIX1; E6AP.
Molecular weightCalculated MW: 101 kDa; Observed MW: 90 kDa
Uniprot ID Q05086
Gene ID 7337
StorageShipped on wet ice. Store at -20℃. Stable for 12 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
Precautions[KD Validated] Anti-UBE3A Mouse mAb [55K42K03] is for research use only and not for use in diagnostic or therapeutic procedures.
Background This gene encodes an E3 ubiquitin-protein ligase, part of the ubiquitin protein degradation system. This imprinted gene is maternally expressed in brain and biallelically expressed in other tissues. Maternally inherited deletion of this gene causes Angelman Syndrome, characterized by severe motor and intellectual retardation, ataxia, hypotonia, epilepsy, absence of speech, and characteristic facies. The protein also interacts with the E6 protein of human papillomavirus types 16 and 18, resulting in ubiquitination and proteolysis of tumor protein p53. Alternative splicing of this gene results in three transcript variants encoding three isoforms with different N-termini. Additional transcript variants have been described, but their full length nature has not been determined.

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