| Name | PEX2 |
|---|---|
| Synonyms | 35 kDa peroxisomal membrane protein; PAF1; PAF 1; PEX 2; PEX2; PMP 3; PMP3; PMP35… |
| Name | nonanol |
|---|---|
| CAS | 3,5,5-trimethyl-1-hexanol |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 9270878 | Tateishi K, Okumoto K, Shimozawa N, Tsukamoto T, Osumi T, Suzuki Y, Kondo N, Okano I, Fujiki Y: Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals. Eur J Cell Biol. 1997 Aug;73(4):352-9. We isolated peroxisome biogenesis mutants from Chinese hamster ovary (CHO) cells, using the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/ UV) method and wild-type CHO-K1 cells that had been stably transfected with cDNA encoding Pex2p (formerly peroxisome assembly factor-1, PAF-1). |
6(0,0,1,1) | Details |
| 10441330 | Toyama R, Mukai S, Itagaki A, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Wanders RJ, Fujiki Y: Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants. Hum Mol Genet. 1999 Sep;8(9):1673-81. We isolated peroxisome biogenesis mutants ZP128 and ZP150 from rat PEX2 -transformed Chinese hamster ovary (CHO) cells, by the 9-(1'-pyrene) nonanol/ultraviolet method. |
6(0,0,1,1) | Details |
| 10222139 | Ghaedi K, Itagaki A, Toyama R, Tamura S, Matsumura T, Kawai A, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y: Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals. Exp Cell Res. 1999 May 1;248(2):482-8. We isolated peroxisome biogenesis-defective mutants from rat PEX2-transformed Chinese hamster ovary (CHO) cells, using the 9-(1'-pyrene) nonanol/ultraviolet method. |
6(0,0,1,1) | Details |
| 10222140 | Ghaedi K, Kawai A, Okumoto K, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y: Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein. Exp Cell Res. 1999 May 1;248(2):489-97. We developed an improved method for isolation of peroxisome biogenesis-defective somatic animal cell mutants, using a combination of green fluorescent protein (GFP) expression and the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/UV) selection method. By transfection of PEX2, PEX5, PEX6, and PEX12 cDNAs and cell fusion analysis between the CHO cell mutants, five different complementation groups (CGs) were identified. |
1(0,0,0,1) | Details |
| 9184070 | Okumoto K, Bogaki A, Tateishi K, Tsukamoto T, Osumi T, Shimozawa N, Suzuki Y, Orii T, Fujiki Y: Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III. Exp Cell Res. 1997 May 25;233(1):11-20. We made use of the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/UV) method and isolated peroxisome-deficient mutant cells. TKa cells, the wild-type Chinese hamster ovary (CHO) cells, CHO-K1, that had been stably transfected with cDNA encoding Pex2p (formerly peroxisome assembly factor-1, PAF-1) were used to avoid frequent isolation of the Z65-type, PEX2-defective mutants. |
1(0,0,0,1) | Details |
| 12054689 | Akiyama N, Ghaedi K, Fujiki Y: A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import. Biochem Biophys Res Commun. 2002 May 24;293(5):1523-9. From mutagenized wild-type CHO-K1 cells stably expressing rat Pex2p and Pex3p (1-40)-EGFP, cell colonies resistant to the 9-(1 (')-pyrene) nonanol/ultraviolet treatment were examined for intracellular location of peroxisomal proteins, including EGFP chimera, catalase, and matrix proteins with PTS types 1 and 2. Genetic defect of ZPEG309 was a nonsense point mutation in a codon for Arg50 in CHO PEX2 and a mutation resulting in a C-terminal truncation of the introduced rat Pex2p. |
1(0,0,0,1) | Details |