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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 25 units | Warenkorb auf Verfügbarkeit prüfen | € 288,00 € 244,80 | |
| 50 units | Warenkorb auf Verfügbarkeit prüfen | € 500,00 | |
| 250 units | Warenkorb auf Verfügbarkeit prüfen | € 1.790,00 |
Über diesen Artikel
CAS-Nummer:
UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
232-652-9
MDL number:
Specific activity:
≥0.05 unit/mg solid (with excess pyridoxal 5-phosphate), <0.005 unit/mg solid (without pyridoxal 5-phosphate)
Biological source:
Streptococcus faecalis
€ 244,80
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Unterstützung erhaltenbiological source
Streptococcus faecalis
Quality Level
form
powder
specific activity
≥0.05 unit/mg solid (with excess pyridoxal 5-phosphate), <0.005 unit/mg solid (without pyridoxal 5-phosphate)
storage temp.
−20°C
Application
L-Tyrosine decarboxylase apoenzyme from Streptococcus faecalis has been used:
Biochem/physiol Actions
Other Notes
Dried cells grown on vitamin B6-deficient medium.
One unit will liberate 1.0 μmole of CO2 from L-tyrosine per min at pH 5.5 at 37 °C.
1 of 1
Dieser Artikel | |||
|---|---|---|---|
| specific activity ≥0.05 unit/mg solid (with excess pyridoxal 5-phosphate), <0.005 unit/mg solid (without pyridoxal 5-phosphate) | specific activity ≥0.1 unit/mg solid | specific activity ≥200 units/mg protein | specific activity - |
| biological source Streptococcus faecalis | biological source - | biological source Porcine heart | biological source - |
| form powder | form powder | form ammonium sulfate suspension | form powder |
| storage temp. −20°C | storage temp. −20°C | storage temp. 2-8°C | storage temp. −20°C |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Verwandter Inhalt
QC Methods
J C Vederas et al.
The Journal of biological chemistry, 254(12), 5053-5057 (1979-06-25)
Sodium boro[3H]hydride reduction of tyrosine decarboxylase from Streptococcus faecalis followed by complete hydrolysis of the enzyme produces epsilon-[3H]pyridoxyllysine. Degradation of this material to [4'-3H]pyridoxamine and stereochemical analysis with apoaspartate aminotransferase shows that the re side at C-4' of the cofactor
T Miura et al.
International journal of cancer, 46(5), 931-934 (1990-11-15)
Phenolic melanin precursors can be utilized for the development of anti-melanoma agents. The sulphur homologue of tyrosine, 4-S-cysteinylphenol (CP) and its decarboxylation product, 4-S-cysteaminylphenol (CAP) were shown to be substrates of melanoma tyrosinase, forming melanin-like pigment. Both, but in particular
Gunsalus, I.C., and Smith, R.A.
Methods in Enzymology, 3, 963-963 (1957)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T7927-50UN | 04061833632482 |
| T7927-250UN | 04061833632468 |
| T7927-25UN | 04061833632475 |



