Coriell Institute
Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Disorders of the Urea Cycle
Class Disorders of Amino Acid Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race Caucasian
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Mexican-American; RBC Arginase deficiency; see GM02011A Lymphoid
Passage Frozen 5
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
arginase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number:
Remark Mexican-American; RBC Arginase deficiency; see GM02011A Lymphoid
Michels VV, Beaudet AL, Arginase deficiency in multiple tissues in argininemia. Clin Genet13:61-7 1978
PubMed ID: 624188
No data is available
Passage Frozen 5
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA

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