1422 Results for: "vac1&amp"

Supplier: Thermo Fisher Scientific

2-Acrylamido-2-methylpropanesulphonic acid ≥98%

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA1 Rabbit Polyclonal Antibody (FITC (Fluorescein))

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA1 Rabbit Polyclonal Antibody

Supplier: Spectrum Chemical

2-Amino-2-methyl-1-propanol, or aminomethyl propanol is a colourless, viscous liquid that functions as a pH adjuster. It is also used as an intermediate in drug synthetic schemes.

Supplier: UNITED BIOCHEMICALS

Anti-Amphetamine Mouse Monoclonal Antibody [clone: 10B152]

Supplier: UNITED BIOCHEMICALS

Anti-PRKAG3 Goat Polyclonal Antibody

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA1 Rabbit Polyclonal Antibody

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA1 Mouse Monoclonal Antibody (APC (Allophycocyanin)) [clone: 167CT22.1.6]

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterised by the presence of twelve membrane-spanning domains in its sequences.

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterised by the presence of twelve membrane-spanning domains in its sequences.

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localised to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: BIOSS INC

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA1 Mouse Polyclonal Antibody

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: UNITED BIOCHEMICALS

Anti-PRKAG2 Mouse Monoclonal Antibody [clone: 3C4]

Supplier: UNITED BIOCHEMICALS

Anti-PRKAA2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: UNITED BIOCHEMICALS

Anti-PRKAB1 Rabbit Polyclonal Antibody (PE (Phycoerythrin))

Supplier: BIOSS INC

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.