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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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109 TrueClone belong to pathway "lysine degradation"

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SKUAccnSymbolDescriptionShipping
SC123700BC009580OGDHOGDH (untagged)-Homo sapiens, Similar to oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide), clone MGC:14605 IMAGE:4046929, complete cds0
SC123709BC009362SETDB1SETDB1 (untagged)-Homo sapiens, SET domain, bifurcated 1, clone MGC:15194 IMAGE:4301680, complete cds0
SC319501NM_004092ECHS1ECHS1 (untagged)-Human enoyl CoA hydratase, short chain, 1, mitochondrial (ECHS1), nuclear gene encoding mitochondrial protein0
SC119956NM_000302PLOD1PLOD1 (untagged)-Human procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1 (PLOD1)0
SC309089NM_133331WHSC1WHSC1 (untagged)-Human Wolf-Hirschhorn syndrome candidate 1 (WHSC1), transcript variant 20
SC313085AY102937KMT5A (untagged)-Human SET domain-containing protein 8 (SET8) mRNA, complete cds5
SC111310NM_017778WHSC1L1WHSC1L1 (untagged)-Human Wolf-Hirschhorn syndrome candidate 1-like 1 (WHSC1L1), transcript variant short0
SC126971NM_013976GCDHGCDH (untagged)-Human glutaryl-CoA dehydrogenase (GCDH), nuclear gene encoding mitochondrial protein, transcript variant 24
SC127054NM_031915SETDB2SETDB2 (untagged)-Human SET domain, bifurcated 2 (SETDB2), transcript variant 10
SC127446NM_017635KMT5BSUV420H1 (untagged)-Human suppressor of variegation 4-20 homolog 1 (Drosophila) (SUV420H1), transcript variant 10
SC127702NM_002541OGDHOGDH (untagged)-Human oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) (OGDH), nuclear gene encoding mitochondrial protein, transcript variant 10
SC304570NM_018245OGDHLOGDHL (untagged)-Human oxoglutarate dehydrogenase-like (OGDHL), nuclear gene encoding mitochondrial protein, transcript variant 14
SC308777NM_025256EHMT2EHMT2 (untagged)-Human euchromatic histone-lysine N-methyltransferase 2 (EHMT2), transcript variant NG36/G9a-SPI3
SC308853NM_018489ASH1LASH1L (untagged)-Human ash1 (absent, small, or homeotic)-like (Drosophila) (ASH1L)12
SC316872NM_133330WHSC1WHSC1 (untagged)-Human Wolf-Hirschhorn syndrome candidate 1 (WHSC1), transcript variant 14
SC324589NM_002541OGDHOGDH (untagged)-Human oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) (OGDH), nuclear gene encoding mitochondrial protein, transcript variant 10
SC328603NM_001184797TMLHETMLHE (untagged)-Human trimethyllysine hydroxylase epsilon (TMLHE) nuclear gene encoding mitochondrial protein transcript variant 23
SC329619NM_001201377 ALDH7A1ALDH7A1 (untagged) - Homo sapiens aldehyde dehydrogenase 7 family, member A1 (ALDH7A1), transcript variant 13
SC330127NM_001243491 SETDB1SETDB1 (untagged) - Homo sapiens SET domain, bifurcated 1 (SETDB1), transcript variant 33
SC118906NM_001966EHHADHEHHADH (untagged)-Human enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase (EHHADH), transcript variant 10

 

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