• Product name

    Human Hemoglobin ELISA Kit
    See all Hemoglobin kits
  • Detection method

  • Precision

    Sample n Mean SD CV%
    Overall < 10%
    Sample n Mean SD CV%
    Overall < 10%
  • Sample type

    Serum, Plasma
  • Assay type

    Sandwich (quantitative)
  • Sensitivity

    0.845 ng/ml
  • Range

    6.25 ng/ml - 200 ng/ml
  • Recovery

    Sample specific recovery
    Sample type Average % Range
    Serum > 85 % - %

  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Human
  • Product overview

    Human Hemoglobin ELISA Kit is an in vitro enzyme-linked immunosorbent assay (ELISA) for the quantitative measurement of Hemoglobin levels in human serum and plasma. 

    In this assay the Hemoglobin present in samples reacts with the anti-Hemoglobin antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, anti-Hemoglobin antibodies conjugated with horseradish peroxidase (HRP), are added. These enzyme-labeled antibodies form complexes with the previously bound Hemoglobin. Following another washing step, the enzyme bound to the immunosorbent is assayed by the addition of a chromo­genic substrate, 3,3’,5,5’-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of Hemoglobin in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of Hemoglobin in the test sample. The quantity of Hemoglobin in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.

  • Tested applications

    Suitable for: Sandwich ELISAmore details
  • Platform



  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components 1 x 96 tests
    100X HRP-conjugated anti-Human Hemoglobin antibody 1 x 150µl
    20X Wash Buffer Concentrate 1 x 50ml
    5X Diluent Concentrate 1 x 50ml
    Chromogen Substrate Solution 1 x 12ml
    Human Hemoglobin Calibrator (lyophilized) 1 vial
    Human Hemoglobin ELISA Microplate 1 unit
    Stop Solution 1 x 12ml
  • Research areas

  • Function

    Involved in oxygen transport from the lung to the various peripheral tissues.
  • Tissue specificity

    Red blood cells.
  • Involvement in disease

    Defects in HBA1/HBA2 may be a cause of Heinz body anemias (HEIBAN) [MIM:140700]. This is a form of non-spherocytic hemolytic anemia of Dacie type 1. After splenectomy, which has little benefit, basophilic inclusions called Heinz bodies are demonstrable in the erythrocytes. Before splenectomy, diffuse or punctate basophilia may be evident. Most of these cases are probably instances of hemoglobinopathy. The hemoglobin demonstrates heat lability. Heinz bodies are observed also with the Ivemark syndrome (asplenia with cardiovascular anomalies) and with glutathione peroxidase deficiency.
    Defects in HBA1/HBA2 are the cause of alpha-thalassemia (A-THAL) [MIM:604131]. The thalassemias are the most common monogenic diseases and occur mostly in Mediterranean and Southeast Asian populations. The hallmark of alpha-thalassemia is an imbalance in globin-chain production in the adult HbA molecule. The level of alpha chain production can range from none to very nearly normal levels. Deletion of both copies of each of the two alpha-globin genes causes alpha(0)-thalassemia, also known as homozygous alpha thalassemia. Due to the complete absence of alpha chains, the predominant fetal hemoglobin is a tetramer of gamma-chains (Bart hemoglobin) that has essentially no oxygen carrying capacity. This causes oxygen starvation in the fetal tissues leading to prenatal lethality or early neonatal death. The loss of three alpha genes results in high levels of a tetramer of four beta chains (hemoglobin H), causing a severe and life-threatening anemia known as hemoglobin H disease. Untreated, most patients die in childhood or early adolescence. The loss of two alpha genes results in mild alpha-thalassemia, also known as heterozygous alpha-thalassemia. Affected individuals have small red cells and a mild anemia (microcytosis). If three of the four alpha-globin genes are functional, individuals are completely asymptomatic. Some rare forms of alpha-thalassemia are due to point mutations (non-deletional alpha-thalassemia). The thalassemic phenotype is due to unstable globin alpha chains that are rapidly catabolized prior to formation of the alpha-beta heterotetramers.
    Note=Alpha(0)-thalassemia is associated with non-immune hydrops fetalis, a generalized edema of the fetus with fluid accumulation in the body cavities due to non-immune causes. Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage of a wide variety of disorders.
  • Sequence similarities

    Belongs to the globin family.
  • Post-translational

    The initiator Met is not cleaved in variant Thionville and is acetylated.
  • Information by UniProt
  • Alternative names

    • 3-prime alpha-globin gene
    • A gamma globin
    • Alpha 1 globin
    • Alpha 2 globin
    • Alpha 2 globin chain
    • Alpha globin
    • alpha one globin
    • alpha-1 globin
    • Alpha-globin
    • Beta globin
    • CD113t C
    • CD31
    • Delta globin
    • Erythremia, beta-globin type, included
    • Gamma 1 globin
    • Gamma A hemoglobin
    • Gamma globin
    • Hb F Agamma
    • HBA
    • HBA 1
    • HBA 2
    • HBA T3
    • HBA-T2
    • HBA1
    • HBA2
    • HBB
    • Hbb-y
    • HBD
    • Hbe1
    • HBG
    • HBG 1
    • HBG1
    • HBGA
    • HBGR
    • HBH
    • Hemoglobin alpha 1
    • Hemoglobin alpha 1 chain
    • hemoglobin alpha 1 globin chain
    • hemoglobin alpha 2
    • Hemoglobin alpha chain
    • Hemoglobin alpha locus
    • Hemoglobin alpha locus 1
    • hemoglobin alpha-1 chain
    • Hemoglobin beta
    • Hemoglobin beta chain
    • Hemoglobin beta chain complex
    • Hemoglobin beta locus
    • Hemoglobin gamma
    • Hemoglobin gamma 1 chain
    • Hemoglobin gamma A
    • Hemoglobin gamma A chain
    • Hemoglobin subunit alpha
    • Hemoglobin subunit beta
    • Hemoglobin subunit gamma 1
    • hemoglobin, gamma, regulator of
    • Hemoglobin--gamma locus, 136 alanaine
    • HSGGL1
    • LVV-hemorphin-7
    • Methemoglobinemia, beta-globin type, included
    • MGC126895
    • MGC126897
    • Minor alpha-globin locus
    • PRO2979
    see all
  • Database links


Our Abpromise guarantee covers the use of ab157707 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Sandwich ELISA Use at an assay dependent concentration.


  • Hu hemoglobin measured in biologicals showing quantity (ng) per mL of tested sample.

  • Representative standard curve using ab157707 Hemoglobin Human ELISA Kit.



This product has been referenced in:

  • Sundaravel S  et al. Loss of Function of DOCK4 in Myelodysplastic Syndromes Stem Cells is Restored by Inhibitors of DOCK4 Signaling Networks. Clin Cancer Res N/A:N/A (2019). Read more (PubMed: 31308061) »
  • Atashrazm F  et al. Reduced glucocerebrosidase activity in monocytes from patients with Parkinson's disease. Sci Rep 8:15446 (2018). Read more (PubMed: 30337601) »
See all 6 Publications for this product

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