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- B88bba7d341e9c3774ee36a7e13d294eb NCIT_P378 "NCI" @default.
- B88bba7d341e9c3774ee36a7e13d294eb type Axiom @default.
- B88bba7d341e9c3774ee36a7e13d294eb annotatedProperty IAO_0000115 @default.
- B88bba7d341e9c3774ee36a7e13d294eb annotatedSource NCIT_C18091 @default.
- B88bba7d341e9c3774ee36a7e13d294eb annotatedTarget "Gel electrophoresis is a method of separating large molecules (such as DNA fragments or proteins) from a mixture of similar molecules by electrophoretic filtration through a gelatinous matrix. Subject to an electric field, each molecule in the sample mixture migrates through the matrix at a different rate, depending mainly on electrical charge and size, resulting in spatial separation within the matrix of each molecular species in the sample mixture. Agarose and acrylamide in a cylindrical tube or slab gel are commonly used media for electrophoresis of proteins and nucleic acids." @default.