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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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36 TrueClone belong to pathway "primary bile acid biosynthesis"

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Direct Download
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SKUAccnSymbolDescriptionShipping
SC127431NM_002979SCP2SCP2 (untagged)-Human sterol carrier protein 2 (SCP2), transcript variant 10
SC323038NM_001127610BAATBAAT (untagged)-Human bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase) (BAAT), transcript variant 23
SC328474NM_001167596AMACRAMACR (untagged)-Human alpha-methylacyl-CoA racemase (AMACR) nuclear gene encoding mitochondrial protein transcript variant 43
SC328627NM_001167595AMACRAMACR (untagged)-Human alpha-methylacyl-CoA racemase (AMACR) nuclear gene encoding mitochondrial protein transcript variant 30
SC117937NM_003500ACOX2ACOX2 (untagged)-Human acyl-CoA oxidase 2, branched chain (ACOX2)0
SC325588NM_001142777HSD3B7HSD3B7 (untagged)-Human hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 (HSD3B7), transcript variant 23
SC329505NM_001199291 HSD17B4HSD17B4 (untagged) - Homo sapiens hydroxysteroid (17-beta) dehydrogenase 4 (HSD17B4), transcript variant 14
SC329506NM_001199292 HSD17B4HSD17B4 (untagged) - Homo sapiens hydroxysteroid (17-beta) dehydrogenase 4 (HSD17B4), transcript variant 34
SC110313NM_025193HSD3B7HSD3B7 (untagged)-Human hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 (HSD3B7), transcript variant 10
SC120806NM_006668CYP46A1CYP46A1 (untagged)-Human cytochrome P450, family 46, subfamily A, polypeptide 1 (CYP46A1)0
SC301154NM_001007099SCP2SCP2 (untagged)-Human sterol carrier protein 2 (SCP2), transcript variant 30
SC301155NM_001007100SCP2SCP2 (untagged)-Human sterol carrier protein 2 (SCP2), transcript variant 43
SC112657NM_012254SLC27A5SLC27A5 (untagged)-Human solute carrier family 27 (fatty acid transporter), member 5 (SLC27A5)0
SC112712NM_001701BAATBAAT (untagged)-Human bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase) (BAAT), transcript variant 10
SC335167NM_001278739CYP39A1CYP39A1 (untagged) - Human cytochrome P450, family 39, subfamily A, polypeptide 1 (CYP39A1), transcript variant 32
SC336193NM_001278738CYP39A1CYP39A1 (untagged) - Human cytochrome P450, family 39, subfamily A, polypeptide 1 (CYP39A1), transcript variant 22
SC114150NM_016593CYP39A1CYP39A1 (untagged)-Human cytochrome P450, family 39, subfamily A, polypeptide 1 (CYP39A1)0
SC115040NM_014324AMACRAMACR (untagged)-Human alpha-methylacyl-CoA racemase (AMACR), nuclear gene encoding mitochondrial protein, transcript variant 10
SC125616NM_003956CH25HCH25H (untagged)-Human cholesterol 25-hydroxylase (CH25H)0
SC328420NM_001167598AMACRAMACR (untagged)-Human alpha-methylacyl-CoA racemase (AMACR) nuclear gene encoding mitochondrial protein transcript variant 63

 

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