2964 Results for: "5-Acetylthiophene-2-carboxaldehyde&"
6-[(4-Chlorophenyl)thio]imidazo[2,1-b][1,3]thiazole-5-carboxaldehyde
Supplier: Apollo Scientific
6-[(4-Chlorophenyl)thio]imidazo[2,1-b][1,3]thiazole-5-carboxaldehyde
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1-Methyl-3-(thien-2-yl)-1H-pyrazole-5-carboxaldehyde 97+%
Supplier: Apollo Scientific
1-Methyl-3-(thien-2-yl)-1H-pyrazole-5-carboxaldehyde 97+%
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2-(Cyclopropylmethoxy)pyridine-3-carboxaldehyde 97%
Supplier: Thermo Fisher Scientific
2-(Cyclopropylmethoxy)pyridine-3-carboxaldehyde 97%
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5-Fluoro-1-methyl-1H-indazole-6-carboxaldehyde
Supplier: Apollo Scientific
5-Fluoro-1-methyl-1H-indazole-6-carboxaldehyde
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5-Methylthiophene-2-carboxaldehyde 98%
Supplier: Thermo Fisher Scientific
5-Methylthiophene-2-carboxaldehyde 98%
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2,5-Dimethylthiophene-3-carboxaldehyde 95+%
Supplier: Apollo Scientific
2,5-Dimethylthiophene-3-carboxaldehyde 95+%
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2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxaldehyde ≥98%
Supplier: Apollo Scientific
2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxaldehyde ≥98%
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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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2,5-Dimethyl-1,3-oxazole-4-carboxaldehyde 97%
Supplier: Apollo Scientific
2,5-Dimethyl-1,3-oxazole-4-carboxaldehyde 97%
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5-Methoxy-4-methylindole-3-carboxaldehyde 95%
Supplier: Apollo Scientific
5-Methoxy-4-methylindole-3-carboxaldehyde 95%
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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.
Expand 1 Items
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.
Expand 1 Items
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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2'-Chloro-[1,1'-biphenyl]-4-carboxaldehyde 95%
Supplier: Apollo Scientific
2'-Chloro-[1,1'-biphenyl]-4-carboxaldehyde 95%
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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].
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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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Thiophene-2-carboxaldehyde diethylacetal 95%
Supplier: Apollo Scientific
Thiophene-2-carboxaldehyde diethylacetal 95%
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1-(Thieno[3,2-d]pyrimidin-4-yl)piperidine-4-carboxaldehyde 97%
Supplier: Apollo Scientific
1-(Thieno[3,2-d]pyrimidin-4-yl)piperidine-4-carboxaldehyde 97%
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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.
Expand 1 Items
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].
Expand 1 Items
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].
Expand 1 Items
Anti-HINT1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
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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2-[1-Methyl-5-(trifluoromethyl)pyrazol-3-yl]thiophene-5-carboxaldehyde 97%
Supplier: Apollo Scientific
2-[1-Methyl-5-(trifluoromethyl)pyrazol-3-yl]thiophene-5-carboxaldehyde 97%
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6-(3-Thienyl)pyridine-2-carboxaldehyde 95%
Supplier: Apollo Scientific
6-(3-Thienyl)pyridine-2-carboxaldehyde 95%
Expand 1 Items
5-(3-Chlorophenyl)-3-methylisoxazole-4-carboxaldehyde 95+%
Supplier: Apollo Scientific
5-(3-Chlorophenyl)-3-methylisoxazole-4-carboxaldehyde 95+%
Expand 1 Items
5-(4-Fluorophenyl)furan-2-carboxaldehyde 95+%
Supplier: Apollo Scientific
5-(4-Fluorophenyl)furan-2-carboxaldehyde 95+%
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6-Fluorobenzo[b]thiophene-2-carboxaldehyde 95+%
Supplier: Apollo Scientific
6-Fluorobenzo[b]thiophene-2-carboxaldehyde 95+%
Expand 1 Items
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].