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Glutathione Synthetase Protein (GSS) (AA 1-474) (His tag)

Recombinant Glutathione Synthetase protein expressed in Escherichia coli (E. coli).
Catalog No. ABIN666628

Quick Overview for Glutathione Synthetase Protein (GSS) (AA 1-474) (His tag) (ABIN666628)

Target

See all Glutathione Synthetase (GSS) Proteins
Glutathione Synthetase (GSS)

Protein Type

Recombinant

Origin

  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Source

  • 9
  • 4
  • 1
  • 1
  • 1
Escherichia coli (E. coli)

Application

SDS-PAGE (SDS)

Purity

> 95 %
  • Protein Characteristics

    AA 1-474

    Purification tag / Conjugate

    This Glutathione Synthetase protein is labelled with His tag.

    Sequence

    MATNWGSLLQ DKQQLEELAR QAVDRALAEG VLLRTSQEPT SSEVVSYAPF TLFPSLVPSA LLEQAYAVQM DFNLLVDAVS QNAAFLEQTL SSTIKQDDFT ARLFDIHKQV LKEGIAQTVF LGLNRSDYMF QRSADGSPAL KQIEINTISA SFGGLASRTP AVHRHVLSVL SKTKEAGKIL SNNPSKGLAL GIAKAWELYG SPNALVLLIA QEKERNIFDQ RAIENELLAR NIHVIRRTFE DISEKGSLDQ DRRLFVDGQE IAVVYFRDGY MPRQYSLQNW EARLLLERSH AAKCPDIATQ LAGTKKVQQE LSRPGMLEML LPGQPEAVAR LRATFAGLYS LDVGEEGDQA IAEALAAPSR FVLKPQREGG GNNLYGEEMV QALKQLKDSE ERASYILMEK IEPEPFENCL LRPGSPARVV QCISELGIFG VYVRQEKTLV MNKHVGHLLR TKAIEHADGG VAAGVAVLDN PYPV

    Characteristics

    GSS, 1-474aa, Human, His tag, E.coli

    Purification

    > 95% by SDS-PAGE
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  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    20 mM Tris-HCl buffer ( pH 8.0) containing 1 mM DTT, 10 % glycerol

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

    Glutathione Synthetase (GSS)

    Alternative Name

    Glutathione synthetase/GSS

    Background

    Glutathione synthetase, also known GSS, is the second enzyme in the glutathione biosynthesis pathway. It catalyses the condensation of gamma-glutamylcysteine and glycine, to form glutathione. Defects in GSS are the cause of glutathione synthetase deficiency (GSS deficiency) , also known as 5-oxoprolinuria or pyroglutamic aciduria. It is a severe form characterized by an increased rate of hemolysis and defective function of the central nervous system. Recombinant human GSS protein, fused to His-tag at N-terminus, was expressed in E. coli and purified by using conventional chromatography techniques.

    Molecular Weight

    54.5 kDa (494aa) confirmed by MALDI-TOF

    NCBI Accession

    NP_000169

    Pathways

    Warburg Effect
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