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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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75 TrueClone belong to pathway "histidine metabolism"

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Direct Download
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SKUAccnSymbolDescriptionShipping
SC108094NM_152396METTL6METTL6 (untagged)-Human methyltransferase like 6 (METTL6)0
SC317606NM_018396METTL2BMETTL2B (untagged)-Human methyltransferase like 2B (METTL2B)3
SC322071NM_032649CNDP1CNDP1 (untagged)-Human carnosine dipeptidase 1 (metallopeptidase M20 family) (CNDP1)0
SC334834NM_001301791METTL6METTL6 (untagged) - Human methyltransferase like 6 (METTL6), transcript variant 32
SC119703NM_000690ALDH2ALDH2 (untagged)-Human aldehyde dehydrogenase 2 family (mitochondrial) (ALDH2), nuclear gene encoding mitochondrial protein, transcript variant 10
SC119705NM_000692ALDH1B1ALDH1B1 (untagged)-Human aldehyde dehydrogenase 1 family, member B1 (ALDH1B1), nuclear gene encoding mitochondrial protein0
SC119706NM_000693ALDH1A3ALDH1A3 (untagged)-Human aldehyde dehydrogenase 1 family, member A3 (ALDH1A3)0
SC125389NM_032649CNDP1CNDP1 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human carnosine dipeptidase 1 (metallopeptidase M20 family) (CNDP1)2
SC317410NM_152396METTL6METTL6 (untagged)-Human methyltransferase like 6 (METTL6)3
SC319919NM_001091AOC1ABP1 (untagged)-Human amiloride binding protein 1 (amine oxidase (copper-containing)) (ABP1)0
SC320136NM_001031615ALDH3B2ALDH3B2 (untagged)-Human aldehyde dehydrogenase 3 family, member B2 (ALDH3B2), transcript variant 20
SC333203NM_001272072 AOC1ABP1 (untagged) - Homo sapiens amine oxidase, copper containing 1 (AOC1), transcript variant 113
SC126927NM_000240MAOAMAOA (untagged)-Human monoamine oxidase A (MAOA), nuclear gene encoding mitochondrial protein0
SC314351NM_002112HDCHDC (untagged)-Human histidine decarboxylase (HDC)0
SC321115NM_006895HNMTHNMT (untagged)-Human histamine N-methyltransferase (HNMT), transcript variant 10
SC329680NM_001202560 WBSCR22WBSCR22 (untagged) - Homo sapiens Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 13
SC334353NM_001301792METTL6METTL6 (untagged) - Human methyltransferase like 6 (METTL6), transcript variant 42
SC104291NM_032649CNDP1CNDP1 (untagged)-Human carnosine dipeptidase 1 (metallopeptidase M20 family) (CNDP1)4
SC115807NM_006895HNMTHNMT (untagged)-Human histamine N-methyltransferase (HNMT), transcript variant 10
SC303805NM_006657FTCDFTCD (untagged)-Human formiminotransferase cyclodeaminase (FTCD), transcript variant B3

 

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