H0392
Hemoglobin S, Ferrous Stabilized human
lyophilized powder
Synonym(s):
Sickle cell hemoglobin
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About This Item
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biological source
human
Quality Level
Assay
97-100% (agarose gel electrophoresis)
form
lyophilized powder
technique(s)
electrophoresis: suitable
immunofluorescence: suitable
solubility
H2O: soluble 20 mg/mL
suitability
suitable for electrophoresis and chromatography standard
UniProt accession no.
storage temp.
−20°C
Gene Information
human ... HBB(3043)
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General description
Hemoglobin is the major component of red blood cells, and is responsible for their red color. Its normal concentration in erythrocytes is 34%. Hemoglobin is the most important respiratory protein of vertebrates by virtue of its ability to transport oxygen from the lungs to body tissues, and to facilitate the return transport of carbon dioxide.
has not been tested for functional equivalence against native preparations (unlyophilized ferrous hemoglobins).
Application
Hemoglobin S was used in the determination of fetal hemoglobin by time-resolved immunofluorometric assay.
Packaging
Package size indicates the amount of hemoglobin as determined by the procedure of Drabkin, D.L., J. Biol. Chem., 164, 703 (1946).
Reconstitution
When reconstituted with buffer, gives >90% ferrous hemoglobin.
Disclaimer
RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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U Turpeinen et al.
Clinical chemistry, 38(10), 2013-2018 (1992-10-01)
We have developed a "sandwich"-type time-resolved immunofluorometric assay (IFMA) for fetal hemoglobin (HbF) in hemolysates from adults and newborns, amniotic fluid, and plasma, based on a polyclonal and a monoclonal antibody against human fetal hemoglobin. Microtiter wells are coated with
Brian T Castle et al.
Science advances, 5(3), eaau1086-eaau1086 (2019-03-21)
In sickle cell disease, the aberrant assembly of hemoglobin fibers induces changes in red blood cell morphology and stiffness, which leads to downstream symptoms of the disease. Therefore, understanding of this assembly process will be important for the treatment of
Charles T Quinn et al.
British journal of haematology, 175(4), 724-732 (2016-09-09)
Sickle cell disease (SCD) is a significant healthcare burden worldwide, but most affected individuals reside in low-resource areas where access to diagnostic testing may be limited. We developed and validated a rapid, inexpensive, disposable diagnostic test, the HemoTypeSC
Chromatograms
application for HPLCOur team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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