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(S)-(+)-Methyl-3-hydroxybutyrate ≥98%

Supplier: Thermo Scientific
Description: (S)-(+)-Methyl-3-hydroxybutyrate ≥98%

MSDS Certificates

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(R)-(-)-Methyl-3-hydroxybutyrate ≥98%

Supplier: Thermo Scientific
Description: (R)-(-)-Methyl-3-hydroxybutyrate ≥98%

MSDS Certificates

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Methyl (R)-4-chloro-3-hydroxybutyrate 97%

Catalog Number: (APOSOR932699-5G)
Supplier: Apollo Scientific
Description: Methyl (R)-4-chloro-3-hydroxybutyrate 97%
UOM: 1 * 5 g
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(S)-(+)-Methyl-3-hydroxybutyrate

Supplier: Apollo Scientific
Description: (S)-(+)-Methyl-3-hydroxybutyrate

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(R)-(-)-Methyl-3-hydroxybutyrate

Supplier: Apollo Scientific
Description: (R)-(-)-Methyl-3-hydroxybutyrate

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(S)-Methyl-4-chloro-3-hydroxybutyrate 96%

Supplier: Apollo Scientific
Description: (S)-Methyl-4-chloro-3-hydroxybutyrate 96%

Image Unavailable-BOSSBS-5019R-FITC

Anti-ACAT1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-5019R-FITC)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-A680

Anti-ACAT1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-5019R-A680)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-A647

Anti-ACAT1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-5019R-A647)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-A750

Anti-ACAT1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-5019R-A750)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-CY5.5

Anti-ACAT1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-5019R-CY5.5)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-CY7

Anti-ACAT1 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-5019R-CY7)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-A555

Anti-ACAT1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-5019R-A555)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-A350

Anti-ACAT1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-5019R-A350)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R

Anti-ACAT1 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-5019R)
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].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-5019R-CY3

Anti-ACAT1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-5019R-CY3)
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].
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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