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Spectrin beta Chain, Erythrocyte (SPTB) (AA 703-2137) antibody

SPTB Reactivity: Human, Mouse WB, ELISA, FACS Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7602356
  • Target See all Spectrin beta Chain, Erythrocyte (SPTB) Antibodies
    Spectrin beta Chain, Erythrocyte (SPTB)
    Binding Specificity
    AA 703-2137
    Reactivity
    • 12
    • 1
    • 1
    Human, Mouse
    Host
    • 7
    • 5
    Rabbit
    Clonality
    • 7
    • 5
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Un-conjugated
    Application
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Flow Cytometry (FACS)
    Purpose
    Anti-beta 1 Spectrin/SPTB Antibody Picoband®
    Cross-Reactivity (Details)
    No cross-reactivity with other proteins.
    Characteristics
    Anti-beta 1 Spectrin/SPTB Antibody Picoband® (ABIN7602356). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse. 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 beta 1 Spectrin/SPTB recombinant protein (Position: M703-Y2137).
    Isotype
    IgG
    Top Product
    Discover our top product SPTB Primary Antibody
  • Application Notes
    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Basseres, D. S., Duarte, A. S. S., Hassoun, H., Costa, F. F., Saad, S. T. O. Beta-spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism. Brit. J. Haemat. 115: 347-353, 2001. Note: Erratum: Brit. J. Haemat. 116: 925 only, 2002. 2. Basseres, D. S., Vicentim, D. L., Costa, F. F., Saad, S. T. O., Hassoun, H. Beta-spectrin Promissao: a translation initiation codon mutation of the beta-spectrin gene (ATG-to-GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian family. (Letter) Blood 91: 368-369, 1998. 3. Becker, P. S., Tse, W. T., Lux, S. E., Forget, B. G. Beta-spectrin Kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1. J. Clin. Invest. 92: 612-616, 1993.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Adding 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, 0.2 mg Na2HPO4.
    Storage
    4 °C,-20 °C
    Storage Comment
    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 freezing and thawing.
  • Target
    Spectrin beta Chain, Erythrocyte (SPTB)
    Alternative Name
    SPTB (SPTB Products)
    Background

    Synonyms: Caspase-2, CASP-2, Neural precursor cell expressed developmentally down-regulated protein 2, NEDD-2, Protease ICH-1, Caspase-2 subunit p18, Caspase-2 subunit p13, Caspase-2 subunit p12, CASP2, ICH1, NEDD2

    Tissue Specificity: Expressed at higher levels in the embryonic lung, liver and kidney than in the heart and brain. In adults, higher level expression is seen in the placenta, lung, kidney, and pancreas than in the heart, brain, liver and skeletal muscle.

    Background: Spectrin beta chain, erythrocyte is a protein that in humans is encoded by the SPTB gene. This locus encodes a member of the spectrin gene family. Spectrin proteins, along with ankyrin, play a role in cell membrane organization and stability. The protein encoded by this locus functions in stability of erythrocyte membranes, and mutations in this gene have been associated with spherocytosis type 2, hereditary elliptocytosis, and neonatal hemolytic anemia. Alternatively spliced transcript variants have been described.

    Molecular Weight
    270 kDa
    Gene ID
    6710
    UniProt
    P11277
    Pathways
    Regulation of Actin Filament Polymerization
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