VWR® La-Pha-Pack™, Shell vials with PE plug
Supplier: LA PHA PACK
These vials are preferentially used on instruments of the following manufacturers: Alcott, Gilson, Shimadzu, Waters® (Wisp 96 respectively 48-position carousel).
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Amp'd® ELISA signal amplification kit
Supplier: ENZO LIFE SCIENCES
Amp'd® ELISA Signal Amplification Kit provides up to 50-fold increase in sensitivity over traditional ELISAs while detecting lower concentrations of target in samples.
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Adenosine-5'-monophosphoric acid (AMP), Wasser_6 99% Dry weight
Supplier: Thermo Fisher Scientific
a useful ligand determinant that facilitate the binding of APS reductase inhibitors and activates adenosine receptor agonists.
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Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
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
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-AMP Activated Protein Kinase alpha1/2 Mouse Monoclonal Antibody [clone: 9E22]
Supplier: US Biological
Anti-AMP Activated Protein Kinase alpha1/2 Mouse Monoclonal Antibody [clone: 9E22]
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Amp'd® glp-1 elisa kit, grow cells
Supplier: ENZO LIFE SCIENCES
Ultra-sensitive AMP'D® GLP-1 ELISA kit enabling the ability to use less sample to detect levels of human Glucagon-like peptide 1 (7-36) amide, a potent promoter of insulin secretion, a major incretin hormone, and therapeutic for type 2 diabetes.
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Anti-AMPD3 Rabbit Polyclonal Antibody (Cy7®)
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® 350)
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 (FITC (Fluorescein Isothiocyanate))
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-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
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-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
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 characterised 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-AMP Activated Protein Kinase 1, 2 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-AMP Activated Protein Kinase 1, 2 Rabbit Polyclonal Antibody
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Cyclic AMP Select ELISA Kit
Supplier: Cayman Chemical
For direct quantification of cAMP from a variety of biological samples.
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Anti-Cyclic AMP Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-Cyclic AMP Rabbit Polyclonal Antibody
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Anti-Cyclic AMP Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-Cyclic AMP Rabbit Polyclonal Antibody
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VWR® Screw Neck Vials, ND40
Supplier: VWR Collection
Cylindrical vial made of clear glass, 3rd hydrol. class.
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Sample vials in Lab File®, WHEATON®
Supplier: DWK Life Sciences
Clear vials made from low extractable borosilicate glass, amber vials made from borosilicate glass.
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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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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-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® 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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Amp'd® HSP70 high sensitivity ELISA Kit
Supplier: ENZO LIFE SCIENCES
Ultra-sensitive (7 pg/ml)Amp'd® HSP70 high sensitivity ELISA kit enabling the ability to use less sample and detect both baseline and upregulated levels of human, mouse and rat Hsp70 (Hsp72), a major chaperone, cancer biomarker, and key cell stress regulator.
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Anti-HINT1 Rabbit Polyclonal Antibody (Cy5®)
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-AMPD3 Rabbit Polyclonal Antibody (Cy5®)
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 (Cy3®)
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.
Expand 1 Items
Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
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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Labtop coolers, Nalgene®
Supplier: Thermo Fisher Scientific
Labtop coolers −20 °C.
PC, blue.
Lower section filled with a non toxic gel, with handle.
471-0000/471-0001: Will maintain a temperature below –15 °C for up to 2 hours.
Sixteen inserts included convert 1,5 ml holes to accept either 0,5 or 0,2 ml tubes.