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OriGene in recent publications
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis Nat. Neurosci. 664-6 17 5. May 2014 [MATR3]

Fungal engagement of the C-type lectin mincle suppresses dectin-1-induced antifungal immunity Cell Host Microbe 494-505 15 4. April 2014 [CLEC4E]

Proteome-wide epitope mapping of antibodies using ultra-dense peptide arrays Mol. Cell Proteomics. April 2014 [MKNK2]

Proteome-wide epitope mapping of antibodies using ultra-dense peptide arrays Mol. Cell Proteomics. April 2014 [RNF214]

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9 Protein belong to family "ion channels: potassium"

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SKUAccnSymbolDescriptionShipping
TP302421NM_004823KCNK6Recombinant protein of human potassium channel, subfamily K, member 6 (KCNK6)In Stock
TP306124NM_002236KCNF1Recombinant protein of human potassium voltage-gated channel, subfamily F, member 1 (KCNF1)In Stock
TP306399NM_031460KCNK17Recombinant protein of human potassium channel, subfamily K, member 17 (KCNK17), transcript variant 1In Stock
TP310184NM_000890KCNJ5Recombinant protein of human potassium inwardly-rectifying channel, subfamily J, member 5 (KCNJ5)In Stock
TP310938NM_002240KCNJ6Recombinant protein of human potassium inwardly-rectifying channel, subfamily J, member 6 (KCNJ6)In Stock
TP313421NM_172163KCNQ4Recombinant protein of human potassium voltage-gated channel, KQT-like subfamily, member 4 (KCNQ4), transcript variant 2In Stock
TP313846NM_033310KCNK4Recombinant protein of human potassium channel, subfamily K, member 4 (KCNK4)In Stock
TP316336NM_004983KCNJ9Recombinant protein of human potassium inwardly-rectifying channel, subfamily J, member 9 (KCNJ9)In Stock
TP322200NM_004974KCNA2Recombinant protein of human potassium voltage-gated channel, shaker-related subfamily, member 2 (KCNA2)In Stock

 

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