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  • Journal
    Digital Access
    Provider
    Version
    Ovid
    31st., 2023
    Ovid
    30th., 2022
    Ovid
    29th ed., 2021
    Ovid
    28th ed., 2020
    Ovid
    27th ed., 2019
    Ovid
    26th ed., 2018
    Ovid
    25th ed., 2017
    Ovid
    23rd ed., 2015
    Print Access Request
    Location
    Version
    Call Number
    Items
    Books: General Collection (Downstairs)
    2015-18.
    RC55 .A14
    4
  • Article
    Rosenblum BB, Merritt AD.
    Am J Hum Genet. 1978 Jul;30(4):434-41.
    The genetic heterogeneity of human pancreatic alpha-amylase (alpha-1,4-glucan 4-glucanohydrolase, E.C. 3.2.1.1) has been better defined through the development of an asparagine buffered electrophoretic gel system. Three alleles had been identified for the pancreatic amylase locus, AMY2, with two variant alleles as autosomal dominant traits on Tris HCl buffered sheet gels. The asparagine buffered sheet gel now allows the differentiation of the genotypes AMY2B/AMY2B,AMY2B/AMY2A, and AMY2B/AMY2C, thus classifying these three alleles as codominants. Asparagine buffered polyacrylamide gels and thin layer polyacrylamide isoelectric focusing aided in the identification of three new pancreatic amylase variants: AMY2D,AMY2E, and AMY2F. AMY2E has been identified only in AMY2B and AMY2E individuals. This allele is proposed as a quantitative activity variant with essentially the same electrophoretic mobility as AMY2A. The other new autosomal variants have each been identified in single white families. AMY2D is dominant and AMY2F is a codominant trait as shown on thin layer polyacrylamide isoelectric focusing gels.
    Digital Access Access Options