G6PD polyclonal, anti-human
€428.00
In stock
SKU
BS90548
Catalog Number: BS90548
Size: 100 µl
Other Size: 50 µl
Isotype: rabbit IgG
Applications: WB, ICC, IF, IHC, FC
Questions? Contact us!
Size: 100 µl
Other Size: 50 µl
Isotype: rabbit IgG
Applications: WB, ICC, IF, IHC, FC
Questions? Contact us!
Background:
Glucose-6-phosphate isomerase (GPI) has many other names, including Phosphohexose isomerase (PHI), Neuroleukin (NLK) and Spermantigen-36 (SA-36). GPI is a cytoplasmic homodimer belonging to the GPI family. It is a neurotrophic factor for spinal and sensory neurons and is involved in glycolysis and gluconeogenesis. Defects or mutations in GPI can cause hereditary nonspherocytic hemolytic anemia (HA), hydrops fetalis, immediate neonatal death and neurological impairment.
Alternative Name:
GPI, AMF, NLK, PGI, PHI, SA-36, AMF, Aurocrine motility factor, Autocrine motility factor, DKFZp686C13233, EC 5.3.1.9, G6PI, Glucose phosphate isomerase, Glucose-6-phosphate isomerase, GNPI, GPI, Gpi1, Hexose monophosphate isomerase, Hexosephosphate isomerase, Neuroleukin, NLK, Oxoisomerase, PGI, PHI, Phosphoglucose isomerase, Phosphohexomutase, Phosphohexose isomerase, Phosphosaccharomutase, SA 36, SA-36, SA36,
Application Dilution:
WB:1:500-1:1,000
ICC:1:50-1:200
IHC:1:50-1:200
FC:1:50-1:100
Specificity: G6PD polyclonal antibody detects endogenous levels of G6PD protein.
Immunogen:
Recombinant protein corresponding to human Glucose 6 phosphate isomerase 300-500aa.
MW: 63 kDa
Swiss-Prot: P06744(Human)
Purification & Purity:
ProA affinity purified
Format:
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Storage:
Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.
For research use only, not for use in diagnostic procedure.
Glucose-6-phosphate isomerase (GPI) has many other names, including Phosphohexose isomerase (PHI), Neuroleukin (NLK) and Spermantigen-36 (SA-36). GPI is a cytoplasmic homodimer belonging to the GPI family. It is a neurotrophic factor for spinal and sensory neurons and is involved in glycolysis and gluconeogenesis. Defects or mutations in GPI can cause hereditary nonspherocytic hemolytic anemia (HA), hydrops fetalis, immediate neonatal death and neurological impairment.
Alternative Name:
GPI, AMF, NLK, PGI, PHI, SA-36, AMF, Aurocrine motility factor, Autocrine motility factor, DKFZp686C13233, EC 5.3.1.9, G6PI, Glucose phosphate isomerase, Glucose-6-phosphate isomerase, GNPI, GPI, Gpi1, Hexose monophosphate isomerase, Hexosephosphate isomerase, Neuroleukin, NLK, Oxoisomerase, PGI, PHI, Phosphoglucose isomerase, Phosphohexomutase, Phosphohexose isomerase, Phosphosaccharomutase, SA 36, SA-36, SA36,
Application Dilution:
WB:1:500-1:1,000
ICC:1:50-1:200
IHC:1:50-1:200
FC:1:50-1:100
Specificity: G6PD polyclonal antibody detects endogenous levels of G6PD protein.
Immunogen:
Recombinant protein corresponding to human Glucose 6 phosphate isomerase 300-500aa.
MW: 63 kDa
Swiss-Prot: P06744(Human)
Purification & Purity:
ProA affinity purified
Format:
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Storage:
Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.
For research use only, not for use in diagnostic procedure.
| Is Featured? | No |
|---|
Write Your Own Review