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Merck

H0138

Sigma-Aldrich

Haptoglobin Human, Phenotype 1-1

98-100%, essentially salt-free, lyophilized powder

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About This Item

Número de CAS:
MDL number:
UNSPSC Code:
12352202
NACRES:
NA.61

biological source

human

Quality Level

assay

98-100%

form

essentially salt-free, lyophilized powder

technique(s)

cell culture | mammalian: suitable

capacity

≥0.5 mg/mg (hemoglobin)

solubility

H2O: soluble 10 mg/mL

UniProt accession no.

storage temp.

2-8°C

Gene Information

human ... HP(3240)

Other Notes

Occurs as 3 major phenotypes: type 1-1, type 2-1, type 2-2.

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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SNA delegates study COAR recommendations.
C Grimaldi et al.
The American nurse, 21(5), 5-5 (1989-05-01)
Margherita Maffei et al.
BMC biology, 7, 87-87 (2009-12-19)
Obesity is a chronic low inflammatory state. In the obesity condition the white adipose tissue (WAT) is massively infiltrated with monocytes/macrophages, and the nature of the signals recruiting these inflammatory cells has yet to be fully elucidated. Haptoglobin (Hp) is
Eiko Shimada et al.
Transfusion, 47(12), 2315-2321 (2007-09-04)
Congenital haptoglobin deficiency is a risk factor for anaphylactic nonhemolytic transfusion reactions in Japan. The deleted allele of the haptoglobin gene, Hp(del), which causes congenital haptoglobin deficiency, has also been observed in other Northeast Asian populations, such as Korean and
Laust Dupont et al.
Progress in transplantation (Aliso Viejo, Calif.), 27(4), 386-391 (2017-12-01)
Cardiovascular disease is the leading cause of death in renal transplant recipients. An association between haptoglobin genotype 2-2 and cardiovascular disease has been found in patients with diabetes mellitus and liver transplant recipients. To date, the role of haptoglobin genotype
Juan A Moreno et al.
Arteriosclerosis, thrombosis, and vascular biology, 30(6), 1253-1262 (2010-03-20)
In addition to its role in the clearance of haptoglobin-hemoglobin (Hp-Hb) complexes, CD163 is a macrophage scavenger receptor for tumor necrosis factor-like weak inducer of apoptosis (TWEAK). We recently reported that the CD163/TWEAK plasma ratio could be a potential biomarker

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