
Thermo Fisher Scientific MUTYH Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
2 µg/mL
Immunohistochemistry (IHC)
1:10-1:2,000
Immunocytochemistry (ICC/IF)
18 µg/mL
Product Specifications
Species Reactivity
Bacteria, Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
A synthetic peptide corresponding to amino acids 531-546 of human MYH. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MUTYH,
uniProtId:
Q9UIF7-1,
ncbiNodeId:
9606,
antigenRange:
531-546,
antigenLength:
546,
antigenImageFileName:
PA1-41003_MUTYH_Q9UIF7-1_Rabbit.svg,
antigenImageFileNamePDP:
PA1-41003_MUTYH_Q9UIF7-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Protein G
Storage buffer
PBS with 0.05% BSA
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2147401
Product Specific Information
Suggested positive control: Hela whole cell extract.
Target Information
MYH (mutY homolog (E. coli )) is a DNA glycosylase mismatch repair enzyme that in conjunction with mutM (OGG1), cleaves adenine residues paired with either oxidized (8-hydroxyguanines) or non-modified guanines in order to correct A/G and A/C mismatches. Repair of most modified and mispaired bases in the genome is initiated by DNA glycosylases, which bind and cleave N-glycosyl bonds to initiate base excision repair. MYH is crucial for the avoidance of mutations resulting from oxidative DNA damage. Multiple N-terminal splice variants of MYH exist in mammalian cells. Increasing levels of MYH in A549 cells exposed to oxygen and infrared radiation leads to improvements in cell survival. Biallelic MYH germ-line mutations predispose humans to colorectal adenomas and carcinomas. MYH is abundant in neurons where mitochondrial genomes exposed to reactive oxygen species (ROS) that damage DNA must maintain integrity over the entire mammalian life span.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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