Cystathionase (CTH) Human Recombinant Protein
CAT#: TP724814
Recombinant Human Cystathionine r-Lyase/CTH
Need it in bulk or customized? Get a free quote |
CNY 3,140.00
货期*
详询
规格
Product images
![](https://cdn.origene.com/img/defaults-img.jpg)
经常一起买 (1)
CTH (Cystathionase) mouse monoclonal antibody, clone OTI1E12 (formerly 1E12)
CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Species | Human |
Protein Source | E. coli |
Expression cDNA Clone or AA Sequence |
Met1-Ser405
|
Buffer | Supplied as a 0.2 um filtered solution of PBS, 500mM NaCl, 20%Glycerol, pH7.4 |
Note | Recombinant Human Cystathionine Gamma-Lyase is produced by our E.coli expression system and the target gene encoding Met1-Ser405 is expressed. |
Storage | Store at ≤-70°C, stable for 6 months after receipt.Store at ≤-70°C, stable for 3 months under sterile conditions after opening.Please minimize freeze-thaw cycles. |
Stability | 12 months from date of despatch |
Reference Data | |
Locus ID | 1491 |
UniProt ID | P32929 |
Synonyms | Cystathionine Gammaâ€Lyase, Cysteineâ€Protein Sulfhydrase, Gammaâ€Cystathionase, CTH |
Summary | Cystathionine Gamma-Lyase (CTH) is the member of the trans-sulfuration enzymes family. CTH can form homotetramers and interacts with CALM in a calcium-dependent manner. CTH catalyzes the breakdown of cystathionine into cysteine, ammonia and 2-oxobutanoate. CTH also plays an important role in the last step in the trans-sulfuration pathway from methionine to cysteine and has broad substrate specificity. Defects in CTH lead to cystathioninuria, which is an autosomal recessive phenotype characterized by abnormal accumulation of plasma cystathionine. |
Protein Pathways | Cysteine and methionine metabolism, Glycine, serine and threonine metabolism, Metabolic pathways, Nitrogen metabolism, Selenoamino acid metabolism |
Documents
FAQs |
SDS |
其它Cystathionase产品
Customer
Reviews
Loading...