MPG Polyclonal Antibody
€0.00
In stock
SKU
E-AB-14767
Catalog Number: E-AB-14767
Isotype: Rabbit IgG
Reactivity: human
Applications: WB,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human
Applications: WB,ELISA
Datasheet, Questions? Contact us!
Background:
Maintenance of DNA sequences is necessary for vertebrates and other life. DNA is under constant stress by a plethora of DNA-damaging agents present in both the environment and within cells. The potentially deleterious effects of DNA lesions in cells are elegantly resolved by sophisticated DNA repair systems, including base excision repair (BER), nucleotide excision repair (NER) and DNA repair methyltransferase (MTase). Methylated bases, such as 3-methyladenine (3MeA) and 7-methylguanine (7MeG) can be formed by agents in the environment and by endogenous cellular processes. Consequently, in the absence of exposure to environmental agents, DNA methylation damage can be incurred on the genomic DNA of normal mammalian cells. DNA N-glycosylases are base excision-repair proteins that locate and cleave damaged bases from DNA as the first step in restoring the sequence.
Research Area: Epigenetics and Nuclear Signaling
Synonyms:
3 alkyladenine DNA glycosylase, 3-alkyladenine DNA glycosylase, 3-methyladenine DNA glycosidase, 3MG, AAG, ADPG, Alkyladenine DNA glycosylase, anpg, APNG, CRA36.1, DNA 3 methyladenine glycosylase, DNA-3-methyladenine glycosylase, MDG, Mid1, Mpg, N methylpurine DNA glycosirase, N methylpurine DNA glycosylase, N-methylpurine-DNA glycosylase, PIG11, PIG16, Proliferation inducing protein 11, Proliferation inducing protein 16
Immunogen: Recombinant protein of human MPG
Swissprot: P29372
Gene Accession: BC014991
Calculated MW: 32 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.7 mg/mL
Dilution: WB 1:1000-1:5000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-21446/sc-292808
Maintenance of DNA sequences is necessary for vertebrates and other life. DNA is under constant stress by a plethora of DNA-damaging agents present in both the environment and within cells. The potentially deleterious effects of DNA lesions in cells are elegantly resolved by sophisticated DNA repair systems, including base excision repair (BER), nucleotide excision repair (NER) and DNA repair methyltransferase (MTase). Methylated bases, such as 3-methyladenine (3MeA) and 7-methylguanine (7MeG) can be formed by agents in the environment and by endogenous cellular processes. Consequently, in the absence of exposure to environmental agents, DNA methylation damage can be incurred on the genomic DNA of normal mammalian cells. DNA N-glycosylases are base excision-repair proteins that locate and cleave damaged bases from DNA as the first step in restoring the sequence.
Research Area: Epigenetics and Nuclear Signaling
Synonyms:
3 alkyladenine DNA glycosylase, 3-alkyladenine DNA glycosylase, 3-methyladenine DNA glycosidase, 3MG, AAG, ADPG, Alkyladenine DNA glycosylase, anpg, APNG, CRA36.1, DNA 3 methyladenine glycosylase, DNA-3-methyladenine glycosylase, MDG, Mid1, Mpg, N methylpurine DNA glycosirase, N methylpurine DNA glycosylase, N-methylpurine-DNA glycosylase, PIG11, PIG16, Proliferation inducing protein 11, Proliferation inducing protein 16
Immunogen: Recombinant protein of human MPG
Swissprot: P29372
Gene Accession: BC014991
Calculated MW: 32 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.7 mg/mL
Dilution: WB 1:1000-1:5000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-21446/sc-292808
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