GPI antibody (AA 401-500) (FITC)
Quick Overview for GPI antibody (AA 401-500) (FITC) (ABIN1710512)
Target
See all GPI AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 401-500
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Cross-Reactivity
- Mouse
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Predicted Reactivity
- Human,Rat,Dog,Cow,Pig,Horse
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human Glucose 6 phosphate isomerase
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Isotype
- IgG
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Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
- 12 months
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- GPI (Glucose-6-Phosphate Isomerase (GPI))
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Alternative Name
- GPI
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Background
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Synonyms: Glucose 6 phosphate isomerase, AMF, Aurocrine motility factor, Autocrine motility factor, DKFZp686C13233, EC 5.3.1.9, G6PI_HUMAN, Glucose phosphate isomerase, Glucose-6-phosphate isomerase, GNPI, GPI, Gpi1, Hexose monophosphate isomerase, Hexosephosphate isomerase, Neuroleukin, NLK, Oxoisomerase, PHI, Phosphoglucose isomerase, Phosphohexomutase, Phosphohexose isomerase, Phosphosaccharomutase, SA 36, SA-36, SA36, Sperm antigen 36.
Background: This gene belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways. The protein encoded by this gene is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate and fructose-6-phosphate. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. [provided by RefSeq, Jul 2008].
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Gene ID
- 51701
Target
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