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Anti-Glucose 6 Phosphate Dehydrogenase, ALEXA Fluor 594

Anti-Glucose 6 Phosphate Dehydrogenase, ALEXA Fluor 594 size: 100 microliters 489

Supplier BIOSS POLYCLONAL ANTIBODIES
Price 489
Size 100 microliters
Contact us Ask Component cell markers and DNA bp. markers are genetic markerser genes or DNA sequenceswith selection audit
TypeConjugated Primary Antibody
Conjugated with 594, ALEXA FLUOR®
Host organismRabbit (Oryctolagus cuniculus)
Target Protein/PeptideGlucose 6 Phosphate Dehydrogenase
SpecificityThis antibody reacts specifically with Glucose 6 Phosphate Dehydrogenase
ModificationNo modification has been applied to this antibody
Modification siteNone
ClonalityPolyclonal Antibody
ClonePolyclonal Antibodies
Concentration1ug per 1ul
Subcellular locationsN/A
Antigen SourceKLH conjugated synthetic peptide derived from human Glucose 6 Phosphate Dehydrogenase
Gene ID2539
Swiss ProtN/A
ApplicationsIF(IHC-P)
Applications with corresponding dilutionsIF(IHC-P)(1:50-200)
Cross reactive species Mouse (Mus musculus), Rat (Rattus norvegicus), Human (Homo sapiens)
Cross Reactive Species details However, note that due to limited knowledge it is impossible to predict with 100% guarantee that the antibody does not corss react with any other species, No significant cross reactivity has been observed for this antibody for the tested species
Background information Class-I variants are associated with severe NSHA, Deficiency of G6PD is associated with hemolytic anemia in two different situations, First, G6PD-deficiency alleles have reached high frequencies (1% to 50%) and deficient individuals, Secondly, Several types of CNSHA are recognized, and they usually present a more severe phenotype, class-II have an activity <, class-III have an activity of 10% to 60% of normal, class-IV have near normal activity, have a high risk of acute hemolytic attacks, in areas in which malaria has been endemic, sporadic cases of G6PD deficiency occur at a very low frequencies, though essentially asymptomatic in the steady state, 10% of normal, Defects in G6PD are the cause of chronic non-spherocytic hemolytic anemia (CNSHA)
Purification methodPurified by Protein A
Storage 50% glycerol and 0, Store at 4°, 09% sodium azide, C for 12 months, Water buffered solution containing 100ug/ml BSA
Excitation emission590nm/617nm
Synonyms G6PD1, G6PD_HUMAN, G6pdx, Glucose 6 phosphate 1 dehydrogenase, Glucose-6-phosphate 1-dehydrogenase, MET19, POS10, Zwf1p, G6PD
Also known asGlucose 6 Phosphate Dehydrogenase Antibody
Other nameAnti-Glucose 6 Phosphate Dehydrogenase
Advisory For antibodies that are in liquid form or reconstituted lyophilized antibodies small amounts could become entrapped on the seal or the walls of the tube, Prior to use briefly centrifuge the vial to gather all the solution on the bottom, specificity and sensitivity, thus reducing its reactivity, Avoid freeze/thaw cycles as they may denaturate the polypeptide chains of the antibody
PropertiesFor facs or microscopy Alexa 1 conjugate
ConjugationAlexa Fluor
Gene targetGlucose 6 Phosphate Dehydrogenase
Short name Fluor 594, Anti-Glucose 6 Phosphate Dehydrogenase
LabelALEXA
Alternative name ALEXA Fluor 594, antibody to-Glucose 6 Phosphate Dehydrogenase

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