1830 Results for: "Hastelloy+C®+alloy&amp"

Supplier: Bioss

AMP deaminase plays a critical role in energy metabolism.

Supplier: Bioss

Probable inhibitory regulator of the Ras-cyclic AMP pathway.

Supplier: Bioss

Probable inhibitory regulator of the Ras-cyclic AMP pathway.

Supplier: Avantor Fluid Handling

AMP TERMINAL 41560 1 * 1 items

Supplier: US Biological

Anti-PRKAG1 Rabbit Polyclonal Antibody

Supplier: Bioss

Probable inhibitory regulator of the Ras-cyclic AMP pathway.

Supplier: VWR Collection

Stainless steel. Wire weights up to 500 mg in cobalt alloy.

Supplier: ENZO LIFE SCIENCES

Cell-permeable, potent and AMP-competitive inhibitor of glycogen phosphorylase.

Supplier: US Biological

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

Supplier: US Biological

Anti-AK1 Mouse Monoclonal Antibody [clone: 3A6-1F5]

Supplier: R L ENTERPRISES

Alloy/zinc plated steel construction.

Supplier: Avantor Fluid Handling

GF Signet REPL. ROTOR PIN HASTELLOY C 1 * 1 items

Supplier: US Biological

Anti-AK3 Rabbit Polyclonal Antibody

Supplier: Cayman Chemical

Cyclic AMP 1 * 1 g

Supplier: Cayman Chemical

Cyclic AMP 1 * 5 g

Supplier: VWR Collection

CIRCUIT BOARD ASSY AMP 1 * 1 items

Supplier: Bioss

ATP + L-aspartate + tRNA(Asp) = AMP + diphosphate + L-aspartyl-tRNA(Asp).

Supplier: Bioss

ATP + L-aspartate + tRNA(Asp) = AMP + diphosphate + L-aspartyl-tRNA(Asp).

Supplier: VWR Collection

Labomeca Rod Alloy 16X1000mm 1 * 5 items

Supplier: Heidolph Instruments GmbH & Co.KG

The Hei-PLATE Mix 20 L magnetic stirrer without heating function is ideal for applications up to 20 L and can gently stir your solution in a speed range of 100 to 1400 min⁻¹.

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.

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.

Supplier: US Biological

Anti-ATF6 Goat Polyclonal Antibody

Supplier: ELMA SCHMIDBAUER

Powerful cleaners for ultrasonic baths suitable for many industrial cleaning tasks

Supplier: R L ENTERPRISES

Double bosshead made from cast alloy.

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.

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.

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.

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.

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.