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Merck
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MAK115

Sigma-Aldrich

Hemoglobin Assay Kit

sufficient for 250 colorimetric tests

Sinónimos:

Hemoglobin Quantitation Kit

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About This Item

Código UNSPSC:
12161503
NACRES:
NA.84

uso

sufficient for 250 colorimetric tests

método de detección

colorimetric

enfermedades relevantes

hematological disorder

temp. de almacenamiento

2-8°C

Información sobre el gen

human ... HBA1(3039) , HBA2(3040) , HBB(3043)
mouse ... HBB(15129)
rat ... HBB(24440)

Categorías relacionadas

Descripción general

Hemoglobin (Hb) is an iron-containing metalloprotein that serves as the primary means of oxygen transport in vertebrates. Hemoglobin is primarily found in red blood cells where it makes up to 97% of the cell′s dry content. Hemoglobin can also be found in other tissues where it serves as an antioxidant. Alterations in blood hemoglobin levels occurs in many diseases such as anemia and polycytheima.

Aplicación

Hemoglobin Assay Kit has been used to measure the concentration of hemoglobin.

Características y beneficios

Compatible with high-throughput handling systems. Can be adapted for use with cuvettes.

Idoneidad

Suitable for the detection of hemoglobinin a variety of samples such as blood, serum, plasma, and urine. This kit can be used to study the effects of various compounds on hemoglobin metabolism and levels.

Principio

This assay is based on the improved Triton™[NP1]/NaOH method in which hemoglobin is converted to a colorimetric product measured at 400 nm. This assay has a linear detection range between 0.9-200 mg/dL in the 96 well plate assay.

Información legal

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

Pictogramas

CorrosionEnvironment
GHS05,GHS09

Palabra de señalización

Warning

Frases de peligro

H290,H319,H410

Clasificaciones de peligro

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Met. Corr. 1

Código de clase de almacenamiento

8B - Non-combustible corrosive hazardous materials

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Certificados de análisis (COA)

Lot/Batch Number
115CE11A22
115CE07A03
115CE02A22
115CE07A03
115CE11A22

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Diamond-Blackfan anemia (DBA) is a rare, inherited bone marrow failure syndrome, characterized by red blood cell aplasia, developmental abnormalities, and enhanced risk of malignancy. However, the underlying pathogenesis of DBA is yet to be understood. Recently, mutations in the gene
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Replacement therapy is the most common treatment for reduction of bleeding and control of episodic bleeding in individuals with hemophilia. Despite the proven effectiveness of factor replacement therapy, repeated intravenous administration is a heavy burden to individuals with hemophilia. To
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International Journal of Inflammation, 2014 (2014)
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