3042 Results for: "AMARELL, ARNO&"
Anti-LIPT1 Rabbit Polyclonal Antibody
Supplier: ProSci Inc.
The process of transferring lipoic acid to proteins is a two-step process. The first step is the activation of lipoic acid by lipoate-activating enzyme to form lipoyl-AMP. For the second step, LIPT1 transfers the lipoyl moiety to apoproteins.The process of transferring lipoic acid to proteins is a two-step process. The first step is the activation of lipoic acid by lipoate-activating enzyme to form lipoyl-AMP. For the second step, the protein encoded by this gene transfers the lipoyl moiety to apoproteins. Alternative splicing in the 5' UTR of this gene results in five transcript variants that encode the same protein.
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Anti-NUDT9 Rabbit Polyclonal Antibody
Supplier: ProSci Inc.
NUDT9 hydrolyzes ADP-ribose (ADPR) to AMP and ribose 5'-phosphate.
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SureSwab Rapid Multiple Drug Test Kit
Supplier: SURESCREEN
SureSwab rapid kit is quick and easy form of oral drug screening.
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Anti-PRKAA2 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA2 Rabbit Polyclonal Antibody
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Anti-PRKAA1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody
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Single-Phase Input Variable-Speed Controllers
Supplier: Avantor Fluid Handling
Operate a 230-240 VAC motor with only a 115 VAC power supply.
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Anti-AK5 Mouse Polyclonal Antibody
Supplier: US Biological
Anti-AK5 Mouse Polyclonal Antibody
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Anti-PRKAG1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAG1 Rabbit Polyclonal Antibody
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Anti-CREB3 Mouse Monoclonal Antibody [clone: 3H5]
Supplier: US Biological
Anti-CREB3 Mouse Monoclonal Antibody [clone: 3H5]
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Anti-CYTH2 Rabbit Polyclonal Antibody (Biotin)
Supplier: US Biological
Anti-CYTH2 Rabbit Polyclonal Antibody (Biotin)
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Anti-AMPK1, 2 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-AMPK1, 2 Rabbit Polyclonal Antibody
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Anti-ADCY1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
This is a calmodulin-sensitive adenylyl cyclase. May be involved in regulatory processes in the central nervous system. It may play a role in memory acquisition and learning. Plays a role in the regulation of the circadian rhythm of daytime contrast sensitivity probably by modulating the rhythmic synthesis of cyclic AMP in the retina (By similarity).
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Anti-IMPAD1 Rabbit Polyclonal Antibody
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
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.
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Anti-ADCY7 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
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.
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Anti-ADCY7 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
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.
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Drug testing kit for surfaces
Supplier: SURESCREEN
Using the swab and buffer, this kit allows swabbing of suspect surfaces or powders to determine if they are amphetamines.
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Anti-AK5 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-AK5 Rabbit Polyclonal Antibody
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)
Supplier: Bioss
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.
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Anti-IMPAD1 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
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.
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Anti-ADCY1 Rabbit Polyclonal Antibody
Supplier: Bioss
This is a calmodulin-sensitive adenylyl cyclase. May be involved in regulatory processes in the central nervous system. It may play a role in memory acquisition and learning. Plays a role in the regulation of the circadian rhythm of daytime contrast sensitivity probably by modulating the rhythmic synthesis of cyclic AMP in the retina (By similarity).