UNG Protein (GST tag)
Aperçu rapide pour UNG Protein (GST tag) (ABIN7317329)
Antigène
Voir toutes UNG ProtéinesType de proteíne
Origine
Source
Pureté
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Purification/Conjugué
- Cette UNG protéine est marqué à la GST tag.
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Fonction
- Recombinant Human Uracil-DNA glycosylase/UNG Protein (GST Tag)
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Séquence
- Phe 85-Leu 304
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Attributs du produit
- A DNA sequence encoding the human UNG isoform 1 (P13051-2) (Phe 85-Leu 304) was fused with the GST tag at the N-terminus.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Please refer to the printed manual for detailed information.
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Buffer
- Lyophilized from sterile 40 mM Tris, 0.15M NaCl, 2 mM GSH, pH 7.5
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Stock
- 4 °C,-20 °C,-80 °C
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Stockage commentaire
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
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- UNG (Uracil-DNA Glycosylase (UNG))
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Autre désignation
- Uracil-DNA glycosylase/UNG
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Classe de substances
- Viral Protein
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Sujet
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Background: Isoform 1 is widely expressed with the highest expression in skeletal muscle, heart and testicles. Isoform 2 has the highest expression levels in tissues containing proliferating cells. Uracil-DNA glycosylase exists in two forms: mitochondrial uracil-DNA glycosylase 1 (UNG1) and nuclear uracil-DNA glycosylase 2 (UNG2). uracil-DNA glycosylase. This gene encodes one of several uracil-DNA glycosylases. One important function of uracil-DNA glycosylases is to prevent mutagenesis by eliminating uracil from DNA molecules by cleaving the N-glycosylic bond and initiating the base-excision repair (BER) pathway. Uracil bases occur from cytosine deamination or misincorporation of dUMP residues. Alternative promoter usage and splicing of this gene leads to two different isoforms: the mitochondrial UNG1 and the nuclear UNG2. The UNG2 term was used as a previous symbol for the CCNO gene (GeneID 10309), which has been confused with this gene, in the literature and some databases. Defects in UNG are a cause of immunodeficiency with hyper-IgM type 5 (HIGM5). A rare immunodeficiency syndrome characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE. It results in a profound susceptibility to bacterial infections.
Synonym: DGU,HIGM4,HIGM5,UDG,UNG1,UNG15,UNG2
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Poids moléculaire
- 52 kDa
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Pathways
- Réparation de l'ADN, Production of Molecular Mediator of Immune Response
Antigène
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