39051 Results for: "Zaragatoas+para+limpeza&"
Anti-PRKAA1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
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2-Acrylamido-2-methylpropanesulphonic acid ≥98%
Supplier: Thermo Fisher Scientific
2-Acrylamido-2-methylpropanesulphonic acid ≥98%
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Anti-PRKAA1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody
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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-Amphetamine Mouse Monoclonal Antibody [clone: 10B152]
Supplier: US Biological
Anti-Amphetamine Mouse Monoclonal Antibody [clone: 10B152]
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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®
Supplier: Merck
AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®
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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-PRKAA1 Rabbit Polyclonal Antibody (FITC (Fluorescein))
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody (FITC (Fluorescein))
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Ethanol 20% (w/w), Emprove® Expert for cleaning biochromatography resins, SAFC®
Supplier: MERCK PRODUCTION CHEMICALS
Ethanol 20% (w/w), Emprove® Expert for cleaning biochromatography resins, SAFC®
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Dibutyryl-cAMP sodium salt ≥97.0% (by HPLC)
Supplier: TCI
Dibutyryl-cAMP sodium salt ≥97.0% (by HPLC)
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Anti-PRKAA1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody
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Anti-PRKAA1 Mouse Monoclonal Antibody (APC (Allophycocyanin)) [clone: 167CT22.1.6]
Supplier: US Biological
Anti-PRKAA1 Mouse Monoclonal Antibody (APC (Allophycocyanin)) [clone: 167CT22.1.6]
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Anti-PRKAG3 Goat Polyclonal Antibody
Supplier: US Biological
Anti-PRKAG3 Goat Polyclonal Antibody
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Anti-PRKAB2 Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))
Supplier: US Biological
Anti-PRKAB2 Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))
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VWR® Puranity PU, Catridges and Accessories
Supplier: VWR Collection
Filter cartridge, VWR®, Cleaning solution, 1 syringe (disinfection cartridge required), for PU
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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®
Supplier: Merck
AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®
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Anti-PRKAA1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA1 Rabbit Polyclonal Antibody
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Anti-PRKAA1 Mouse Polyclonal Antibody
Supplier: US Biological
Anti-PRKAA1 Mouse Polyclonal Antibody
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Anti-CREB3L1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
Supplier: US Biological
Anti-CREB3L1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
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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-ADCY7 Rabbit Polyclonal Antibody (Cy3®)
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 characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].
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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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
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.
Expand 1 Items
Anti-ADCY7 Rabbit Polyclonal Antibody (Cy5.5®)
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 characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].