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CTH Protein, Human, Recombinant

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Catalog No. TMPJ-00939
Alias γ-Cystathionase, Gamma-Cystathionase, Cysteine-Protein Sulfhydrase, Cystathionine γ-Lyase, Cystathionine Gamma-Lyase, CTH

Cystathionine Gamma-Lyase (CTH) belongs to the trans-sulfuration enzymes family. CTH exists as a homotetramer and interacts with CALM in a calcium-dependent manner. CTH breaks down cystathionine into cysteine, ammonia and 2-oxobutanoate. CTH catalyzes the last step in the trans-sulfuration pathway from methionine to cysteine and has broad substrate specificity. Defects in CTH will lead to cystathioninuria, which is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine.

CTH Protein, Human, Recombinant
Other Forms of CTH Protein, Human, Recombinant:

CTH Protein, Human, Recombinant

😃Good
Catalog No. TMPJ-00939Alias γ-Cystathionase, Gamma-Cystathionase, Cysteine-Protein Sulfhydrase, Cystathionine γ-Lyase, Cystathionine Gamma-Lyase, CTH
Cystathionine Gamma-Lyase (CTH) belongs to the trans-sulfuration enzymes family. CTH exists as a homotetramer and interacts with CALM in a calcium-dependent manner. CTH breaks down cystathionine into cysteine, ammonia and 2-oxobutanoate. CTH catalyzes the last step in the trans-sulfuration pathway from methionine to cysteine and has broad substrate specificity. Defects in CTH will lead to cystathioninuria, which is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine.
Pack SizePriceAvailabilityQuantity
10 μg$116 7-10 days
50 μg$352 7-10 days
500 μg$1,900 7-10 days
1 mg$2,730 7-10 days
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Product Introduction

Bioactivity
Description
Cystathionine Gamma-Lyase (CTH) belongs to the trans-sulfuration enzymes family. CTH exists as a homotetramer and interacts with CALM in a calcium-dependent manner. CTH breaks down cystathionine into cysteine, ammonia and 2-oxobutanoate. CTH catalyzes the last step in the trans-sulfuration pathway from methionine to cysteine and has broad substrate specificity. Defects in CTH will lead to cystathioninuria, which is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine.
Aliasγ-Cystathionase, Gamma-Cystathionase, Cysteine-Protein Sulfhydrase, Cystathionine γ-Lyase, Cystathionine Gamma-Lyase, CTH
Chemical Properties
Molecular Weight38-50 KDa (reducing condition)
Storage & Solubility Information
Storagestore at low temperature | Shipping with blue ice.

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