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Merck
모든 사진(2)

주요 문서

H0392

Sigma-Aldrich

Hemoglobin S, Ferrous Stabilized human

lyophilized powder

동의어(들):

Sickle cell hemoglobin

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About This Item

CAS Number:
MDL number:
UNSPSC 코드:
12352202
eCl@ss:
42030116
NACRES:
NA.61

생물학적 소스

human

Quality Level

분석

97-100% (agarose gel electrophoresis)

양식

lyophilized powder

기술

electrophoresis: suitable
immunofluorescence: suitable

solubility

H2O: soluble 20 mg/mL

적합성

suitable for electrophoresis and chromatography standard

UniProt 수납 번호

저장 온도

−20°C

유전자 정보

human ... HBB(3043)

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

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).

애플리케이션

Hemoglobin S was used in the determination of fetal hemoglobin by time-resolved immunofluorometric assay.

포장

Package size indicates the amount of hemoglobin as determined by the procedure of Drabkin, D.L., J. Biol. Chem., 164, 703 (1946).

재구성

When reconstituted with buffer, gives >90% ferrous hemoglobin.

면책조항

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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이미 열람한 고객

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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
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
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™ , based

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