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Human HP / Haptoglobin Protein - LS-G19958

Catalog Size Price
LS-G19958-200 200 µg Unavailable
LS-G19958-1 1 mg Unavailable
LS-G19958-10 10 mg Unavailable

Most Popular HP / Haptoglobin Proteins

Human HP / Haptoglobin Protein (Recombinant His) - LS-G2813
E. coli Expression System
352 AA
His
Purified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human HP / Haptoglobin Protein (Native) - LS-G5294
Human Expression System
None
Purified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human HP / Haptoglobin Protein (Native) - LS-G5298
Human Expression System
None
Purified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human HP / Haptoglobin Protein (Native) - LS-G5299
Human Expression System
None
Purified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human HP / Haptoglobin Protein (Recombinant His) (aa44-157) - LS-G12901
E. coli Expression System
His
Purified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image

100% Guaranteed
LS-G19958
HP / Haptoglobin
Human
200.0 kDa
Human Haptoglobin produced from pooled human plasma corresponding to the Mw of isotypes of Haptoglobin at 86kD and >200kD.
Human
None
Greater than 96%
Not Tested
Not Tested
Lyophilized from 0.02 M NH4HCO3.
Store at 4°C.
For research use only.

About HP / Haptoglobin

P00738 NM_005143 NP_005134.1

HP Protein, Binding peptide Protein, Haptoglobin alpha(1S)-beta Protein, Haptoglobin, beta polypeptide Protein, Haptoglobin Protein, Haptoglobin alpha(2FS)-beta Protein, Haptoglobin, alpha polypeptide Protein, HP2ALPHA2 Protein, BP Protein, Zonulin Protein, HPA1S Protein

HP / Haptoglobin is a preproprotein, which is processed to yield both alpha and beta chains, which subsequently combine as a tetramer to produce haptoglobin. Haptoglobin functions to bind free plasma hemoglobin, which allows degradative enzymes to gain access to the hemoglobin, while at the same time preventing loss of iron through the kidneys and protecting the kidneys from damage by hemoglobin. Mutations in this gene and/or its regulatory regions cause ahaptoglobinemia or hypohaptoglobinemia.

Requested From: 
Date Requested: 8/22/2017

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