You Searched For: 3,3-Dimethylbutyraldehyde


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Description: α-Acetyl-γ-butyrolactone ≥98%
Catalog Number: B22967.36
UOM: 1 * 500 g
Supplier: Thermo Fisher Scientific

MSDS


Description: α-Acetyl-γ-butyrolactone 99+%
Catalog Number: ACRO102491000
UOM: 1 * 100 mL
Supplier: Thermo Fisher Scientific

MSDS


Description: (S)-tert-Butyl-3-hydroxybutanoate 95%
Catalog Number: APOSOR905870-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: (S)-2-Hydroxybutanoic acid 96%
Catalog Number: APOSOR912658-1G
UOM: 1 * 1 g
Supplier: Apollo Scientific


Description: Ethyl (R)-(-)-4-cyano-3-hydroxybutyate 98%
Catalog Number: L19771.14
UOM: 1 * 25 g
Supplier: Thermo Fisher Scientific

Description: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number: BOSSBS-2698R-CY3
UOM: 1 * 100 µl
Supplier: Bioss


Description: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number: BOSSBS-2698R-A647
UOM: 1 * 100 µl
Supplier: Bioss


Description: This gene encodes a mitochondrially localised enzyme that catalyses the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterised by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.
Catalog Number: BOSSBS-5019R-A680
UOM: 1 * 100 µl
Supplier: Bioss


Description: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number: BOSSBS-2698R-A350
UOM: 1 * 100 µl
Supplier: Bioss


Description: (S)-(+)-Ethyl-3-hydroxybutyrate
Catalog Number: J63184.03
UOM: 1 * 1 g
Supplier: Thermo Fisher Scientific

Description: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
Catalog Number: BOSSBS-5019R-A647
UOM: 1 * 100 µl
Supplier: Bioss


Description: A sensitive tool for measuring β-HB levels in plasma, serum, or urine.
Catalog Number: CAYM700190-96
UOM: 1 * 1 items
Supplier: Cayman Chemical


Description: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number: BOSSBS-2698R-FITC
UOM: 1 * 100 µl
Supplier: Bioss


Description: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
Catalog Number: BOSSBS-5019R-CY5.5
UOM: 1 * 100 µl
Supplier: Bioss


Description: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
Catalog Number: BOSSBS-5019R-CY7
UOM: 1 * 100 µl
Supplier: Bioss


Description: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number: BOSSBS-2698R-A488
UOM: 1 * 100 µl
Supplier: Bioss