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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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361 TrueClone belong to family "ion channels: other"

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  Page: 1 of 19 
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SKUAccnSymbolDescriptionShipping
SC102570NM_015166MLC1MLC1 (untagged)-Human megalencephalic leukoencephalopathy with subcortical cysts 1 (MLC1), transcript variant 10
SC108885NM_001095ASIC1ASIC1 (untagged)-Human amiloride-sensitive cation channel 2, neuronal (ACCN2), transcript variant 20
SC109907NM_172159KCNAB1KCNAB1 (untagged)-Human potassium voltage-gated channel, shaker-related subfamily, beta member 1 (KCNAB1), transcript variant 30
SC116402NM_005971FXYD3FXYD3 (untagged)-Human FXYD domain containing ion transport regulator 3 (FXYD3), transcript variant 10
SC121943NM_198098AQP1AQP1 (untagged)-Human aquaporin 1 (Colton blood group) (AQP1), transcript variant 10
SC121946NM_001680FXYD2FXYD2 (untagged)-Human FXYD domain containing ion transport regulator 2 (FXYD2), transcript variant a0
SC121957NM_001002914KCTD11KCTD11 (untagged)-Human potassium channel tetramerisation domain containing 11 (KCTD11)0
SC121958NM_005031FXYD1FXYD1 (untagged)-Human FXYD domain containing ion transport regulator 1 (FXYD1), transcript variant a4
SC122063NM_152387KCTD18KCTD18 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human potassium channel tetramerisation domain containing 18 (KCTD18)0
SC122090NM_000725CACNB3CACNB3 (untagged)-Human calcium channel, voltage-dependent, beta 3 subunit (CACNB3), transcript variant 10
SC122096NM_173562KCTD20KCTD20 (untagged)-ORIGENE UNIQUE VARIANT 2 of Human potassium channel tetramerisation domain containing 20 (KCTD20)4
SC122112NM_173195KCNIP2KCNIP2 (untagged)-Human Kv channel interacting protein 2 (KCNIP2), transcript variant 63
SC122116NM_002978SCNN1DSCNN1D (untagged)-ORIGENE UNIQUE VARIANT 1 of Human sodium channel, nonvoltage-gated 1, delta (SCNN1D),0
SC122121NM_173562KCTD20KCTD20 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human potassium channel tetramerisation domain containing 20 (KCTD20)0
SC122135NM_201572CACNB2CACNB2 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human calcium channel, voltage-dependent, beta 2 subunit (CACNB2),0
SC122139NM_002978SCNN1DSCNN1D (untagged)-Human sodium channel, nonvoltage-gated 1, delta (SCNN1D), transcript variant 20
SC122144NM_031954KCTD10KCTD10 (untagged)-ORIGENE UNIQUE VARIANT 2 of Human potassium channel tetramerisation domain containing 10 (KCTD10)0
SC122189NM_000727CACNG1CACNG1 (untagged)-Human calcium channel, voltage-dependent, gamma subunit 1 (CACNG1)0
SC122192NM_181671PITPNC1PITPNC1 (untagged)-Human phosphatidylinositol transfer protein, cytoplasmic 1 (PITPNC1), transcript variant 24
SC122202NM_031954KCTD10KCTD10 (untagged)-ORIGENE UNIQUE VARIANT 1 of Human potassium channel tetramerisation domain containing 10 (KCTD10)0

 

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