Magnesium 99.9+% (trace metals basis), turnings
Supplier: Thermo Fisher Scientific
Magnesium 99.9+% (trace metals basis), turnings
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Magnesium chloride hexahydrate 99% for analysis
Supplier: Thermo Fisher Scientific
Magnesium chloride hexahydrate 99% for analysis
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Magnesium oxide ≥99.95% (metals basis)
Supplier: Thermo Fisher Scientific
Magnesium oxide ≥99.95% (metals basis)
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Magnesium oxide ≥99.998% (metals basis), Puratronic®
Supplier: Thermo Fisher Scientific
Magnesium oxide ≥99.998% (metals basis), Puratronic®
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Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
The protein encoded by this gene can hydrolyse substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumour suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene.
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Anti-HINT1 Rabbit Polyclonal Antibody
Supplier: Bioss
The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].
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Anti-AMP Activated Protein Kinase alpha1/AMPKa2 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-AMP Activated Protein Kinase alpha1/AMPKa2 Rabbit Polyclonal Antibody
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Magnesium ≥99.8% (metals basis), turnings
Supplier: Thermo Fisher Scientific
Magnesium ≥99.8% (metals basis), turnings
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Magnesium chloride, ultra dry ≥99.99% (metals basis)
Supplier: Thermo Fisher Scientific
Magnesium chloride, ultra dry ≥99.99% (metals basis)
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Anti-HINT1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].
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Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].
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Magnesium lactate trihydrate ≥99%
Supplier: Thermo Fisher Scientific
White to off-white powder/lumps
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Magnesium aluminate ≥99% (metals basis)
Supplier: Thermo Fisher Scientific
Magnesium aluminate ≥99% (metals basis)
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Magnesium ≥99.9% (metals basis), foil, hard, Thickness: 0.05 mm (0.002 in)
Supplier: Thermo Fisher Scientific
Magnesium ≥99.9% (metals basis), foil, hard, Thickness: 0.05 mm (0.002 in)
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Anti-AMPD3 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
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Glycogen phosphorylase inhibitor ≥99% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Cell-permeable, potent and AMP-competitive inhibitor of glycogen phosphorylase.
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Magnesium oxide ≥99.99% (metals basis)
Supplier: Thermo Fisher Scientific
Magnesium oxide ≥99.99% (metals basis)
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Magnesium diboride ≥99% (metals basis)
Supplier: Thermo Fisher Scientific
Magnesium diboride ≥99% (metals basis)
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Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 488)
Supplier: Bioss
AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
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Anti-AMPD3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
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Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
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Magnesium nitrate solution Reag. Ph. Eur. 1049801
Supplier: VWR Chemicals
The reagent is specially intended for use in testing Ph Eur and monographs. This solution was produced according 4.1.1 of Ph Eur specifications using Ph Eur reagent quality components and water meeting the Ph Eur monograph requirement for Purified Water.
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Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
The protein encoded by this gene can hydrolyse substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumour suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene.
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Magnesium chloride solution 1 M
Supplier: G-Biosciences
Magnesium chloride solution 1 M
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Magnesium(II) gluconate hydrate
Supplier: Thermo Fisher Scientific
Magnesium(II) gluconate hydrate
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Magnesium chloride hexahydrate 98+%, extra pure
Supplier: Thermo Fisher Scientific
Magnesium chloride hexahydrate 98+%, Extra Pure
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Magnesium fluoride hydrate (≥87% MgF₂)
Supplier: Thermo Fisher Scientific
Magnesium fluoride hydrate (≥87% MgF₂)
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Anti-HINT1 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].