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Merck
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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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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
10H7.1, monoclonal
Application:
IHC, WB
Citations:
1
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biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

10H7.1, monoclonal

species reactivity

human

packaging

antibody small pack of 25 μL

technique(s)

immunohistochemistry: suitable (paraffin), western blot: suitable

isotype

IgG2aκ

NCBI accession no.

UniProt accession no.

shipped in

ambient

target post-translational modification

unmodified

Quality Level

Gene Information

human ... UBE3A(7337)

General description

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.
~100 kDa observed; 100.69 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Immunogen

GST/His-tagged recombinant fragment corresponding to 101 amino acids from the internal region of human Ubiquitin-protein ligase E3A.

Application

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.

Biochem/physiol Actions

Clone 10H7.1 detects Ubiquitin-protein ligase E3A in human cells. it targets an epitope with in 101 amino acids from the internal region.

Physical form

Format: Purified

Analysis Note

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.

Other Notes

Concentration: Please refer to lot specific datasheet.

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存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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Andie Dodge et al.
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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