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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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51 TrueClone belong to pathway "one carbon pool by folate"

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SKUAccnSymbolDescriptionShipping
SC310521NM_006636MTHFD2MTHFD2 (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2), nuclear gene encoding mitochondrial protein, transcript variant 13
SC318430NM_015440MTHFD1LMTHFD1L (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L), nuclear gene encoding mitochondrial protein2
SC116397NM_005956MTHFD1MTHFD1 (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase (MTHFD1)0
SC313442NM_175085GARTGART (untagged)-Human phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase (GART), transcript variant 23
SC326924NM_001164710AMTAMT (untagged)-Human aminomethyltransferase (AMT) nuclear gene encoding mitochondrial protein transcript variant 23
SC326943NM_001164712AMTAMT (untagged)-Human aminomethyltransferase (AMT) nuclear gene encoding mitochondrial protein transcript variant 43
SC328792NM_001166357SHMT2SHMT2 (untagged)-Human serine hydroxymethyltransferase 2 (mitochondrial) (SHMT2) transcript variant 33
SC331853NM_001242767 MTHFD1LMTHFD1L (untagged) - Homo sapiens methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L), transcript variant 113
SC111168NM_006636MTHFD2MTHFD2 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2), nuclear gene encoding mitochondrial protein, transc4
SC111221NM_015440MTHFD1LMTHFD1L (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L), nuclear gene encoding mitochondrial protein0
SC120689NM_139242MTFMTMTFMT (untagged)-Human mitochondrial methionyl-tRNA formyltransferase (MTFMT), nuclear gene encoding mitochondrial protein4
SC125742BC015062MTHFD2MTHFD2 (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase, mRNA (cDNA clone MGC:13506 IMAGE:4285669), complete cds3
SC319904NM_005412SHMT2SHMT2 (untagged)-Human serine hydroxymethyltransferase 2 (mitochondrial) (SHMT2), nuclear gene encoding mitochondrial protein, transcript variant 10
SC332908NM_001270364 ALDH1L1ALDH1L1 (untagged) - Homo sapiens aldehyde dehydrogenase 1 family, member L1 (ALDH1L1), transcript variant 113
SC333766NM_001290357DHFRDHFR (untagged) - Human dihydrofolate reductase (DHFR), transcript variant 32
SC317553NM_006636MTHFD2MTHFD2 (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2), nuclear gene encoding mitochondrial protein, transcript variant 13
SC317625NM_139242MTFMTMTFMT (untagged)-Human mitochondrial methionyl-tRNA formyltransferase (MTFMT), nuclear gene encoding mitochondrial protein3
SC323742NM_006636MTHFD2MTHFD2 (untagged)-Human methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2), nuclear gene encoding mitochondrial protein, transcript variant 10
SC337589NM_001291940MTRMTR (untagged) - Human 5-methyltetrahydrofolate-homocysteine methyltransferase (MTR), transcript variant 34
SC330809NM_001270365 ALDH1L1ALDH1L1 (untagged) - Homo sapiens aldehyde dehydrogenase 1 family, member L1 (ALDH1L1), transcript variant 34

 

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