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HBA1 antibody (AA 2-142)

HBA1 Reactivity: Human WB, IHC, FACS Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5518839
  • Target See all HBA1 Antibodies
    HBA1 (Hemoglobin, alpha 1 (HBA1))
    Binding Specificity
    • 12
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2-142
    Reactivity
    • 30
    • 18
    • 4
    • 1
    Human
    Host
    • 35
    • 3
    Rabbit
    Clonality
    • 33
    • 5
    Polyclonal
    Conjugate
    • 20
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HBA1 antibody is un-conjugated
    Application
    • 23
    • 17
    • 10
    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
    Purpose
    Anti-Hemoglobin/HBA1/HBA2 Antibody Picoband®
    Cross-Reactivity (Details)
    No cross-reactivity with other proteins
    Characteristics
    Anti-Hemoglobin/HBA1/HBA2 Antibody Picoband® (ABIN5518839). Tested in Flow Cytometry, IHC, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
    Purification
    Immunogen affinity purified.
    Immunogen
    E.coli-derived human Hemoglobin recombinant protein (Position: V2-R142). Human Hemoglobin shares 85.8% amino acid (aa) sequence identity with mouse Hemoglobin.
    Isotype
    IgG
    Top Product
    Discover our top product HBA1 Primary Antibody
  • Application Notes
    Western blot, 0.1-0.5 μg/mL, Human
    Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human
    Flow Cytometry(Fixed), 1-3 μg/1x106 cells, Human
    1. "Entrez Gene: HBA1 hemoglobin, alpha 1". 2. Stelzl U, Worm U, Lalowski M, Haenig C, Brembeck FH, Goehler H, Stroedicke M, Zenkner M, Schoenherr A, Koeppen S, Timm J, Mintzlaff S, Abraham C, Bock N, Kietzmann S, Goedde A, Toksöz E, Droege A, Krobitsch S, Korn B, Birchmeier W, Lehrach H, Wanker EE (September 2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957-68.
    Comment

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB, supported by ABIN921231 in IHC(P).

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Concentration
    500 μg/mL
    Buffer
    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
    Storage
    4 °C,-20 °C
    Storage Comment
    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Target
    HBA1 (Hemoglobin, alpha 1 (HBA1))
    Alternative Name
    HBA1 (HBA1 Products)
    Background

    Synonyms: Hemoglobin subunit alpha,Alpha-globin,Hemoglobin alpha chain,HBA1,HBA2,

    Tissue Specificity: Red blood cells.

    Background: The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97 % of the total hemoglobin, alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3 % of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1, some nondeletion alpha thalassemias have also been reported.

    Molecular Weight
    15 kDa
    Gene ID
    3039, 3040
    UniProt
    P69905
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