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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]

Glucose-regulated protein 78 autoantibody associates with blood-brain barrier disruption in neuromyelitis optica Sci Transl Med 2017 [HSPA5]

Amplification of F-Actin Disassembly and Cellular Repulsion by Growth Factor Signaling Dev. Cell 2017 [STK38L]

Tyr42 phosphorylation of RhoA GTPase promotes tumorigenesis through nuclear factor (NF)-κB Free Radic. Biol. Med. 2017 [VAV2]

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73 TrueClone belong to pathway "selenoamino acid metabolism"


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SC319344NM_000687AHCYAHCY (untagged)-Human adenosylhomocysteinase (AHCY), transcript variant 10
SC324364NM_000071CBSCBS (untagged)-Human cystathionine-beta-synthase (CBS), transcript variant 10
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
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
SC100504NM_138395MARS2MARS2 (untagged)-Human methionyl-tRNA synthetase 2, mitochondrial (MARS2), nuclear gene encoding mitochondrial protein0
SC302005NM_001015880PAPSS2PAPSS2 (untagged)-Human 3'-phosphoadenosine 5'-phosphosulfate synthase 2 (PAPSS2), transcript variant 23
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
SC128074NM_000071CBSCBS (untagged)-Human cystathionine-beta-synthase (CBS), transcript variant 14
SC302637NM_001032364GGT1GGT1 (untagged)-Human gamma-glutamyltransferase 1 (GGT1), transcript variant 43
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
SC336535NM_001302465GGT5GGT5 (untagged) - Human gamma-glutamyltransferase 5 (GGT5), transcript variant 53
SC336823NM_001288833GGT1GGT1 (untagged) - Human gamma-glutamyltransferase 1 (GGT1), transcript variant 63
SC115457NM_012247SEPHS1SEPHS1 (untagged)-Human selenophosphate synthetase 1 (SEPHS1), transcript variant 10


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