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Hemoglobin antibody

Reactivity: Human WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7134001
  • Target See all Hemoglobin Antibodies
    Hemoglobin
    Reactivity
    • 71
    • 21
    • 14
    • 13
    • 12
    • 8
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Human
    Host
    • 83
    • 35
    • 29
    • 9
    • 4
    • 4
    • 1
    • 1
    Rabbit
    Clonality
    • 125
    • 34
    • 1
    Polyclonal
    Conjugate
    • 64
    • 38
    • 27
    • 21
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Hemoglobin antibody is un-conjugated
    Application
    • 112
    • 99
    • 79
    • 15
    • 12
    • 11
    • 11
    • 10
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Cross-Reactivity
    Human
    Purification
    >95%, Protein G purified
    Immunogen
    Human Hemoglobin protein (Native Protein)
    Isotype
    IgG
    Top Product
    Discover our top product Hemoglobin Primary Antibody
  • Application Notes
    Recommended dilution: WB:1:1000-1:5000,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C,-80 °C
    Storage Comment
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    Hemoglobin
    Abstract
    Hemoglobin Products
    Synonyms
    HGB antibody, Hemoglobin antibody, HGB antibody
    Background

    Background: Hemoglobin is involved in oxygen transport from the lung to the various peripheral tissues. The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult Hemoglobin. The normal adult Hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta zero thalassemia. Reduced amounts of detectable beta globin causes beta plus thalassemia.

    Aliases: Hemoglobin

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