MTHFR 677C>T Reference Standard

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RQPA0019
FormatGenomic DNA
DescriptionMTHFR (Methylenetetrahydrofolate Reductase) is a Protein Coding gene. Diseases associated with MTHFR include Homocystinuria Due To Deficiency Of N -Methylenetetrahydrofolate Reductase Activity and Neural Tube Defects, Folate-Sensitive. Among its related pathways are Metabolism of water-soluble vitamins and cofactors and Carbon metabolism.
  
Technical Data 
GeneMTHFR
AA Changep.A222V
DNA ChangeNM_005957.5_c.667C>T
Chr position (GRCh38)NC_000001.11_g.11796321G>A
Allelic Frequency50%
ZygosityHeterozygous
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencing
Storage4°C
Expiry36 months from the date of manufacture