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OriGene in recent publications
Repurposing of Proton Pump Inhibitors as first identified small molecule inhibitors of endo-β-N-acetylglucosaminidase (ENGase) for the treatment of NGLY1 deficiency, a rare genetic disease Bioorg. Med. Chem. Lett. 2017 [ENGASE]

The lipid moiety 7-ketocholesteryl-9-carboxynonanoate mediates binding interaction of oxLDL to LOX-1 and upregulates ABCA1 expression through PPARγ Life Sci. 2017 [OLR1]

Human GRP78 affinity towards its signaling partners Ire1α and PERK is differently modulated by an unfolded protein client Biochem. Biophys. Res. Commun. 2017 [HSPA5]

Human GRP78 affinity towards its signaling partners Ire1α and PERK is differently modulated by an unfolded protein client Biochem. Biophys. Res. Commun. 2017 [ERN1]

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76 TrueClone belong to pathway "androgen and estrogen metabolism"

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SKUAccnSymbolDescriptionShipping
SC115733NM_007120UGT1A4UGT1A4 (untagged)-Human UDP glucuronosyltransferase 1 family, polypeptide A4 (UGT1A4)0
SC122552NM_000196HSD11B2HSD11B2 (untagged)-Human hydroxysteroid (11-beta) dehydrogenase 2 (HSD11B2)0
SC122715NM_005420SULT1E1SULT1E1 (untagged)-Human sulfotransferase family 1E, estrogen-preferring, member 1 (SULT1E1)0
SC122798NM_014234HSD17B8HSD17B8 (untagged)-Human hydroxysteroid (17-beta) dehydrogenase 8 (HSD17B8)0
SC334731NM_001301790METTL6METTL6 (untagged) - Human methyltransferase like 6 (METTL6), transcript variant 22
SC112141NM_024592SRD5A3SRD5A3 (untagged)-Human steroid 5 alpha-reductase 3 (SRD5A3)0
SC320894NM_017528WBSCR22WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 20
SC119873NM_000413HSD17B1HSD17B1 (untagged)-Human hydroxysteroid (17-beta) dehydrogenase 1 (HSD17B1)0
SC123879NM_000497CYP11B1CYP11B1 (untagged)-Human cytochrome P450, family 11, subfamily B, polypeptide 1 (CYP11B1), nuclear gene encoding mitochondrial protein, transcript variant 10
SC303829NM_006798UGT2A1UGT2A1 (untagged)-Human UDP glucuronosyltransferase 2 family, polypeptide A1, complex locus (UGT2A1)3
SC325935NM_001144767UGT2B10UGT2B10 (untagged)-Human UDP glucuronosyltransferase 2 family, polypeptide B10 (UGT2B10), transcript variant 20
SC336388NM_001301239UGT2A1UGT2A1 (untagged) - Human UDP glucuronosyltransferase 2 family, polypeptide A1, complex locus (UGT2A1), transcript variant 42
SC112983NM_021139UGT2B4UGT2B4 (untagged)-Human UDP glucuronosyltransferase 2 family, polypeptide B4 (UGT2B4)0
SC119463NM_001072UGT1A6UGT1A6 (untagged)-Human UDP glucuronosyltransferase 1 family, polypeptide A6 (UGT1A6), transcript variant 10
SC119466NM_001074UGT2B7UGT2B7 (untagged)-Human UDP glucuronosyltransferase 2 family, polypeptide B7 (UGT2B7)0
SC127812NM_017528WBSCR22WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 20
SC127848NM_000103CYP19A1CYP19A1 (untagged)-Human cytochrome P450, family 19, subfamily A, polypeptide 1 (CYP19A1), transcript variant 10
SC303504NM_004605SULT2B1SULT2B1 (untagged)-Human sulfotransferase family, cytosolic, 2B, member 1 (SULT2B1), transcript variant 13
SC122553NM_000198HSD3B2HSD3B2 (untagged)-Human hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 (HSD3B2), transcript variant 10
SC302654NM_001032391LCMT1LCMT1 (untagged)-Human leucine carboxyl methyltransferase 1 (LCMT1), transcript variant 23

 

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