CTH Protein (AA 1-405)

Produktnummer ABIN1692129

Produktdetails

Target: CTH (Cystathionase (Cystathionine gamma-Lyase) (CTH))

Protein-Typ: Recombinant

Proteineigenschaft: AA 1-405

Spezies: Human

Quelle: Escherichia coli (E. coli)

Verwendungszweck: Recombinant Human Cystathionine γ-Lyase/CTH

Sequenz: GHMQEKDASS QGFLPHFQHF ATQAIHVGQD PEQWTSRAVV PPISLSTTFK QGAPGQHSGF EYSRSGNPTR NCLEKAVAAL DGAKYCLAFA SGLAATVTIT HLLKAGDQII CMDDVYGGTN RYFRQVASEF GLKISFVDCS KIKLLEAAIT PETKLVWIET PTNPTQKVID IEGCAHIVHK HGDIILVVDN TFMSPYFQRP LALGADISMY SATKYMNGHS DVVMGLVSVN CESLHNRLRF LQNSLGAVPS PIDCYLCNRG LKTLHVRMEK HFKNGMAVAQ FLESNPWVEK VIYPGLPSHP QHELVKRQCT GCTGMVTFYI KGTLQHAEIF LKNLKLFTLA ESLGGFESLA ELPAIMTHAS VLKNDRDVLG ISDTLIRLSV GLEDEEDLLE DLDQALKAAH PPSGSHS

Produktmerkmale:

Recombinant Human Cystathionine γ-Lyase/CTH

Reinheit: > 95 % as determined by reducing SDS-PAGE.

Sterilität: 0.2 μm filtered

Endotoxin-Niveau: Less than 0.1 ng/μg (1 IEU/μg) as determined by LAL test

Anwendungsinformationen

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Rekonstitution: It is not recommended to reconstitute to a concentration less than 100 μg/mL.
Dissolve the lyophilized protein in ddH2O.
Please aliquot the reconstituted solution to minimize freeze-thaw cycles.

Buffer: Supplied as a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl,20 % Glycerol, pH 7.4.

Handhabung: Always centrifuge tubes before opening. Do not mix by vortex or pipetting.

Lagerung: -80 °C

Informationen zur Lagerung: Store at < -20°C, stable for 6 months after receipt.
Please minimize freeze-thaw cycles.

Haltbarkeit: 6 months

Antigendetails

Target: CTH (Cystathionase (Cystathionine gamma-Lyase) (CTH))

Andere Bezeichnung: Cystathionine gamma-Lyase/CTH (CTH Produkte)

Hintergrund: Recombinant Human Cystathionine γ-Lyase/CTH is produced with our E. coli expression system. The target protein is expressed with sequence (Met1-Ser405) of Human CTH.
Cystathionine γ-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.

Molekulargewicht: 44.7kDa

UniProt: P32929

Pathways: ER-Nucleus Signaling, Warburg Effekt