MABS1683
Anti-UBE3A Antibody, clone 10H7.1
clone 10H7.1, from mouse
别名:
Ubiquitin-protein ligase E3A, EC: 2.3.2.26, E6AP ubiquitin-protein ligase, HECT-type ubiquitin transferase E3A, Human papillomavirus E6-associated protein, Oncogenic protein-associated protein E6-AP, Renal carcinoma antigen NY-REN-54
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About This Item
生物来源
mouse
质量水平
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
10H7.1, monoclonal
种属反应性
human
包装
antibody small pack of 25 μL
技术
immunohistochemistry: suitable (paraffin)
western blot: suitable
同位素/亚型
IgG2aκ
NCBI登记号
UniProt登记号
运输
ambient
靶向翻译后修饰
unmodified
基因信息
human ... UBE3A(7337)
一般描述
Ubiquitin-protein ligase E3A (UniProt: Q05086; also known as EC: 2.3.2.26, E6AP ubiquitin-protein ligase, HECT-type ubiquitin transferase E3A, Human papillomavirus E6-associated protein, Oncogenic protein-associated protein E6-AP, Renal carcinoma antigen NY-REN-54) is encoded by the UBE3A (also known as E6AP, EPVE6AP, HPVE6A) gene (Gene ID: 7337)in human. UBE3A is the E3 ubiquitin-protein ligase that accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and transfers it to its substrates. Several substrates have been identified, including the RAD23A and RAD23B, MCM7, annexin A1, the PML tumor suppressor, and the cell cycle regulator CDKN1B. UBE3A catalyzes the high-risk human papilloma virus (HPV) E6-mediated ubiquitination of p53/TP53, contributing to the neoplastic progression of cells infected by these viruses. Phosphorylation at Tyr659 by ABL1 impairs E3 ligase activity and protects p53/TP53 from degradation in (HPV)-infected cells. UBE3A may function as a cellular quality control ubiquitin ligase by helping the degradation of the cytoplasmic misfolded proteins and it also promotes its own degradation in vivo. It is reported to plays an important role in the regulation of the circadian clock by ubiquitinating the core clock component ARNTL/BMAL1 and leading to its proteasomal degradation. Three isoforms of UBE3A have been reported that are generated via alternative splicing. Mutations in UBE3A gene cause Angelman syndrome that is characterized by severe motor and intellectual retardation, ataxia, hypotonia, and frequent jerky limb movements.
特异性
Clone 10H7.1 detects Ubiquitin-protein ligase E3A in human cells. it targets an epitope with in 101 amino acids from the internal region.
免疫原
GST/His-tagged recombinant fragment corresponding to 101 amino acids from the internal region of human Ubiquitin-protein ligase E3A.
应用
Anti-UBE3A, clone 10H7.1, Cat. No. MABS1683, is a mouse monoclonal antibody that detects Ubiquitin-protein ligase E3A and is tested for use in Immunohistochemistry (Paraffin) and Western Blotting.
Western Blotting Analysis: A 1:1,000 dilution from a representative lot detected UBE3A in 10 µg of HeLa cell lysate.
Immunohistochemistry Analysis: A 1:1,000 dilution from a representative lot detected UBE3A in human cerebral cortex and human testis tissue.
Immunohistochemistry Analysis: A 1:1,000 dilution from a representative lot detected UBE3A in human cerebral cortex and human testis tissue.
质量
Evaluated by Western Blotting in PC-12 cell lysate.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected UBE3A in 10 µg of PC-12 cell lysate.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected UBE3A in 10 µg of PC-12 cell lysate.
目标描述
~100 kDa observed; 100.69 kDa calculated. Uncharacterized bands may be observed in some lysate(s).
外形
Format: Purified
其他说明
Concentration: Please refer to lot specific datasheet.
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WGK
WGK 1
法规信息
新产品
Autism research : official journal of the International Society for Autism Research, 14(4), 645-655 (2021-01-22)
Disruptions to the maternally inherited allele UBE3A, encoding for an E3 ubiquitin ligase, leads to the manifestation of Angelman Syndrome (AS). While this disorder is rare, the symptoms are severe and lifelong including but not limited to: intractable seizures, abnormal
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