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Homocysteic acid

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Homocysteic acid is a chemical compound that serves as a biochemical intermediate in the metabolism of the amino acid homocysteine. It is often used in research and scientific applications involving the study of amino acid metabolism and related biological processes.

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Lab products found in correlation

Ferrocene, by Merck Group (2 mentions) Sodium citrate, by Santa Cruz Biotechnology (2 mentions) Sodium isocitrate, by Santa Cruz Biotechnology (2 mentions) Sodium succinate, by Santa Cruz Biotechnology (2 mentions) Succinic semialdehyde, by Santa Cruz Biotechnology (2 mentions) Sodium fumarate, by Santa Cruz Biotechnology (2 mentions) Oxaloacetic acid, by Merck Group (2 mentions) Iron acetate, by Merck Group (2 mentions) Cysteine, by Thermo Fisher Scientific (2 mentions) Dimethylsulfoxid, by Thermo Fisher Scientific (2 mentions) Ammonium peroxydisulfate, by Thermo Fisher Scientific (2 mentions) Cis aconitic acid, by Santa Cruz Biotechnology (2 mentions) Sodium α ketoglutarate, by Santa Cruz Biotechnology (2 mentions) L malic acid, by Merck Group (2 mentions) Dl ethionine, by Thermo Fisher Scientific (2 mentions) Nahso3, by Thermo Fisher Scientific (2 mentions) Sodium sulfite na2so3, by Thermo Fisher Scientific (2 mentions) Sodium sulfate na2so4, by Thermo Fisher Scientific (2 mentions) Methionine, by Thermo Fisher Scientific (2 mentions) H3po4, by Merck Group (2 mentions)

2 protocols using homocysteic acid

1

Metabolite Standards for Biochemical Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Metabolite standards were obtained at high purity. If not otherwise indicated, the product number refers to Sigma-Aldrich: sodium citrate (71635), sodium isocitrate (I1252), cis-aconitic acid (A3412), sodium α-ketoglutarate (K2010), sodium succinate (14160), succinic semialdehyde (Santa Cruz Biotechnology, F1114), sodium fumarate (F1506), L-malic acid (M6413), sodium pyruvate (P2256), oxaloacetic acid (O4126), iron acetate (FeAc, 339199), FeCl2 (372870), FeCl3 (157740), Fe(ClO4)2 (334081), Fe(ClO4)3 (309281), ferrocene (F408), FeS(268704), H3PO4 (P5811), 2-mercaptoethanol (Merck Millipore, 805740), cysteine (30095), DL-ethionine (E5139), dimethylsulfoxid (D8418), homocysteic acid (69453), NaHSO3 (Acros Organics, 41944), methionine (M9375), ammonium peroxydisulfate (Fischer Scientific, 10219790), sodium sulfite Na2SO3 (Fischer Scientific, 10070400), sodium sulfate Na2SO4 (Fischer Scientific, 10493372). All water was obtained commercially at UPLC-MS purity (Biosolve Chemicals, Cat no. 23214102).
Keller M.A., Kampjut D., Harrison S.A, & Ralser M. (2017). Sulfate radicals enable a non-enzymatic Krebs cycle precursor. Nature ecology & evolution, 1, 0083.
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2

Metabolite Standards for Biochemical Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Metabolite standards were obtained at high purity. If not otherwise indicated, the product number refers to Sigma-Aldrich: sodium citrate (71635), sodium isocitrate (I1252), cis-aconitic acid (A3412), sodium α-ketoglutarate (K2010), sodium succinate (14160), succinic semialdehyde (Santa Cruz Biotechnology, F1114), sodium fumarate (F1506), L-malic acid (M6413), sodium pyruvate (P2256), oxaloacetic acid (O4126), iron acetate (FeAc, 339199), FeCl2 (372870), FeCl3 (157740), Fe(ClO4)2 (334081), Fe(ClO4)3 (309281), ferrocene (F408), FeS(268704), H3PO4 (P5811), 2-mercaptoethanol (Merck Millipore, 805740), cysteine (30095), DL-ethionine (E5139), dimethylsulfoxid (D8418), homocysteic acid (69453), NaHSO3 (Acros Organics, 41944), methionine (M9375), ammonium peroxydisulfate (Fischer Scientific, 10219790), sodium sulfite Na2SO3 (Fischer Scientific, 10070400), sodium sulfate Na2SO4 (Fischer Scientific, 10493372). All water was obtained commercially at UPLC-MS purity (Biosolve Chemicals, Cat no. 23214102).
Keller M.A., Kampjut D., Harrison S.A, & Ralser M. (2017). Sulfate radicals enable a non-enzymatic Krebs cycle precursor. Nature ecology & evolution, 1, 0083.
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