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2964 results for "5-Acetylthiophene-2-carboxaldehyde&amp"

2964 Results for: "5-Acetylthiophene-2-carboxaldehyde&amp"

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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%

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.

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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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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.

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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-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 (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%

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5-(3-Chlorophenyl)-3-methylisoxazole-4-carboxaldehyde 95+%

Supplier: Apollo Scientific

5-(3-Chlorophenyl)-3-methylisoxazole-4-carboxaldehyde 95+%

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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+%

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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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