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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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73 TrueClone belong to pathway "selenoamino acid metabolism"

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SKUAccnSymbolDescriptionShipping
SC100504NM_138395MARS2MARS2 (untagged)-Human methionyl-tRNA synthetase 2, mitochondrial (MARS2), nuclear gene encoding mitochondrial protein0
SC126889AK090413GGT7 (untagged)-Human mRNA for FLJ00311 protein2
SC326003NM_001130723AHCYL2AHCYL2 (untagged)-Human adenosylhomocysteinase-like 2 (AHCYL2), transcript variant 44
SC326105NM_001130720AHCYL2AHCYL2 (untagged)-Human adenosylhomocysteinase-like 2 (AHCYL2), transcript variant 23
SC314249NM_005443PAPSS1PAPSS1 (untagged)-Human 3'-phosphoadenosine 5'-phosphosulfate synthase 1 (PAPSS1)0
SC320894NM_017528WBSCR22WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 20
SC329999NM_001242673 AHCYL1AHCYL1 (untagged) - Homo sapiens adenosylhomocysteinase-like 1 (AHCYL1), transcript variant 23
SC330001NM_001242675 AHCYL1AHCYL1 (untagged) - Homo sapiens adenosylhomocysteinase-like 1 (AHCYL1), transcript variant 43
SC334731NM_001301790METTL6METTL6 (untagged) - Human methyltransferase like 6 (METTL6), transcript variant 22
SC109271NM_013430GGT1GGT1 (untagged)-Human gamma-glutamyltransferase 1 (GGT1), transcript variant 30
SC127568NM_015328AHCYL2AHCYL2 (untagged)-Human adenosylhomocysteinase-like 2 (AHCYL2), transcript variant 10
SC127812NM_017528WBSCR22WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 20
SC302637NM_001032364GGT1GGT1 (untagged)-Human gamma-glutamyltransferase 1 (GGT1), transcript variant 43
SC324364NM_000071CBSCBS (untagged)-Human cystathionine-beta-synthase (CBS), transcript variant 10
SC336535NM_001302465GGT5GGT5 (untagged) - Human gamma-glutamyltransferase 5 (GGT5), transcript variant 53
SC336823NM_001288833GGT1GGT1 (untagged) - Human gamma-glutamyltransferase 1 (GGT1), transcript variant 63
SC128074NM_000071CBSCBS (untagged)-Human cystathionine-beta-synthase (CBS), transcript variant 14
SC302005NM_001015880PAPSS2PAPSS2 (untagged)-Human 3'-phosphoadenosine 5'-phosphosulfate synthase 2 (PAPSS2), transcript variant 23
SC319344NM_000687AHCYAHCY (untagged)-Human adenosylhomocysteinase (AHCY), transcript variant 10
SC322690NM_001031712TRMT11TRMT11 (untagged)-Human tRNA methyltransferase 11 homolog (S. cerevisiae) (TRMT11)0

 

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