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Recombinant Human Haptoglobin (HP)

The region for expressing recombinant Human HP (Haptoglobin) contains amino acids 19-406. The expected molecular weight for the HP (Haptoglobin) protein is calculated to be 57.3 kDa. The HP (Haptoglobin) protein was expressed in e.coli. The HP (Haptoglobin) gene fragment has been modified by fusing the N-terminal 6xHis-B2M tag, providing convenience in detecting and purifying the recombinant HP (Haptoglobin) protein during the following stages.Human haptoglobin (HP) is a glycoprotein primarily synthesized by the liver and released into the bloodstream. Haptoglobin mainly binds to free hemoglobin, released during the breakdown of red blood cells, preventing oxidative damage and facilitating its clearance by macrophages. This haptoglobin-hemoglobin complex is then efficiently removed from circulation, preventing the harmful effects of free hemoglobin. Beyond its role in hemoglobin scavenging, haptoglobin is involved in immunomodulation and inflammation, influencing processes like the acute-phase response. Additionally, genetic variations in haptoglobin exist, contributing to individual differences in susceptibility to certain diseases. Research on haptoglobin spans various medical fields, including hematology, immunology, and genetics, exploring its multifaceted functions and clinical relevance.

ACP02658

The region for expressing recombinant Human HP (Haptoglobin) contains amino acids 19-406. The expected molecular weight for the HP (Haptoglobin) protein is calculated to be 57.3 kDa. The HP (Haptoglobin) protein was expressed in e.coli. The HP (Haptoglobin) gene fragment has been modified by fusing the N-terminal 6xHis-B2M tag, providing convenience in detecting and purifying the recombinant HP (Haptoglobin) protein during the following stages.Human haptoglobin (HP) is a glycoprotein primarily synthesized by the liver and released into the bloodstream. Haptoglobin mainly binds to free hemoglobin, released during the breakdown of red blood cells, preventing oxidative damage and facilitating its clearance by macrophages. This haptoglobin-hemoglobin complex is then efficiently removed from circulation, preventing the harmful effects of free hemoglobin. Beyond its role in hemoglobin scavenging, haptoglobin is involved in immunomodulation and inflammation, influencing processes like the acute-phase response. Additionally, genetic variations in haptoglobin exist, contributing to individual differences in susceptibility to certain diseases. Research on haptoglobin spans various medical fields, including hematology, immunology, and genetics, exploring its multifaceted functions and clinical relevance.

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Specifications


Cat.No ACP02658 Target NameHP
Target Synonymsalpha polypeptide; Haptoglobin, beta polypeptide; HP; HP2 ALPHA2; HP2ALPHA2; HPA1S; HPT; HPT_HUMAN; MGC111141; Zonulin, Binding peptide; BP; Haptoglobin alpha chain; Haptoglobin alpha(1S) beta; Haptoglobin alpha(2FS) beta; Haptoglobin beta chain; HaptoglobinFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range19-406aa
Mol Weight57.3 kDaProtein LengthFull Length of Mature Protein
PurityGreater than 85% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP00738
Background Information
  • Uniprot Id

    P00738

  • Target Species

    Human

  • Target Name

    HP

  • Target Full Name

    Haptoglobin

  • Target Function

    As a result of hemolysis, hemoglobin is found to accumulate in the kidney and is secreted in the urine. Haptoglobin captures, and combines with free plasma hemoglobin to allow hepatic recycling of heme iron and to prevent kidney damage. Haptoglobin also acts as an antioxidant, has antibacterial activity, and plays a role in modulating many aspects of the acute phase response. Hemoglobin/haptoglobin complexes are rapidly cleared by the macrophage CD163 scavenger receptor expressed on the surface of liver Kupfer cells through an endocytic lysosomal degradation pathway.; The uncleaved form of allele alpha-2 (2-2), known as zonulin, plays a role in intestinal permeability, allowing intercellular tight junction disassembly, and controlling the equilibrium between tolerance and immunity to non-self antigens.

  • Target Involvement

    Anhaptoglobinemia (AHP)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Peptidase S1 family

  • Target Tissue Specificity

    Expressed by the liver and secreted in plasma.

  • Target Research Area

    Immunology, Cardiovascular

  • Target Synonyms

    Binding peptide; BP; Haptoglobin alpha chain; Haptoglobin alpha(1S) beta; Haptoglobin alpha(2FS) beta; Haptoglobin beta chain; Haptoglobin, alpha polypeptide; Haptoglobin, beta polypeptide; HP; HP2 ALPHA2; HP2ALPHA2; HPA1S; HPT; HPT_HUMAN; MGC111141; Zonulin

  • Target Background

    This gene encodes 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. This gene has also been linked to diabetic nephropathy, the incidence of coronary artery disease in type 1 diabetes, Crohn's disease, inflammatory disease behavior, primary sclerosing cholangitis, susceptibility to idiopathic Parkinson's disease, and a reduced incidence of Plasmodium falciparum malaria. The protein encoded also exhibits antimicrobial activity against bacteria. A similar duplicated gene is located next to this gene on chromosome 16. Multiple transcript variants encoding different isoforms have been found for this gene.

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