GCLC Polyclonal Antibody, RBITC Conjugated, Rabbit

Artikelnummer: BSS-BS-23393R-RBITC
Artikelname: GCLC Polyclonal Antibody, RBITC Conjugated, Rabbit
Artikelnummer: BSS-BS-23393R-RBITC
Hersteller Artikelnummer: bs-23393R-RBITC
Alternativnummer: BSS-BS-23393R-RBITC-100
Hersteller: Bioss
Wirt: Rabbit
Kategorie: Antikörper
Applikation: IF, WB
Spezies Reaktivität: Human, Mouse, Rat
Konjugation: RBITC
Alternative Synonym: Gamma ECS, Gamma GCS, Gamma glutamylcysteine synthetase, Gamma-ECS, Gamma-glutamylcysteine synthetase, GCL, GCLC, GCS, GCS Heavy Chain antibody GLCL, GLCLC, GLCLR, Glutamate cysteine ligase catalytic subunit, Glutamate cysteine ligase (gamma glutamylcysteine synthetase) regulatory (30.8kD), Glutamate cysteine ligase catalytic subunit, Glutamate cysteine ligase modifier subunit, Glutamate cysteine ligase regulatory protein, Glutamate cysteine ligase regulatory subunit, Glutamate--cysteine ligase catalytic subunit, GSH1_HUMAN.
The GCLC gene consists of 16 exons and encodes the 636 amino acid protein g-GCSc (g-glutamylcysteine synthetase heavy subunit), also designated g-L-glutamate-L-cysteine ligase catalytic subunit (GLCLC). g-GCSc is expressed in hemocytes, brain, liver and kidney. g-GCSc associates with a regulatory or modifier subunit, g-GCSm (g-glutamylcysteine synthetase light subunit), to form a heterodimer, g-GCS. g-GCS is the first enzyme involved and the rate determining step in glutathione biosynthesis. Oxidants, cadium and methyl mercury upregulate the transcription of g-GCS. H2O2 regulation depends on the Yap1 protein and the presence of glutamate, glutamine and lysine. Cadium regulates transcription through proteins Met-4, Met-31 and Met-32. Cbf1, a DNA binding protein, inhibits transcription of g-GCS. Chemopreventive compounds cause increased levels of g-GCSc in kidney tissues, which may protect against chemically induced carcinogenesis. A His370Leu amino acid change in g-GCSc causes deficiencies in activity which are responsible for hemolytic anemia and low red blood cell glutathione levels. Defects in GCLC are the cause of hemolytic anemia.
Klonalität: Polyclonal
Konzentration: 1ug/ul
NCBI: 2729
UniProt: P48506
Puffer: Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Quelle: KLH conjugated synthetic peptide derived from human GCLC
Target-Kategorie: GCLC
Application Verdünnung: WB(WB=1:500-2000), IF(IF=1:100-500)