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ChT antibody (AA 446-580)

ChT Reactivity: Mouse, Human, Rat WB, FACS, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7601754
  • Target See all ChT Antibodies
    ChT (High Affinity Choline Transporter (ChT))
    Binding Specificity
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 446-580
    Reactivity
    • 8
    • 8
    • 8
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Mouse, Human, Rat
    Host
    • 9
    • 8
    Rabbit
    Clonality
    • 9
    • 8
    Polyclonal
    Conjugate
    • 11
    • 2
    • 2
    • 2
    This ChT antibody is un-conjugated
    Application
    • 8
    • 8
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS), ELISA
    Purpose
    Anti-SLC5A7 Antibody Picoband®
    Cross-Reactivity (Details)
    No cross-reactivity with other proteins.
    Characteristics
    Anti-SLC5A7 Antibody Picoband® (ABIN7601754). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. 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 SLC5A7 recombinant protein (Position: R446-Q580).
    Isotype
    IgG
    Top Product
    Discover our top product ChT Primary Antibody
  • Application Notes
    Western blot, 0.25-0.5 μg/mL/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/mL/1x10^6 cells, Human
    ELISA, 0.1-0.5 μg/mL/mL, Human
    1. Apparsundaram, S., Ferguson, S. M., George, A. L., Jr., Blakely, R. D. Molecular cloning of a human, hemicholinium-3-sensitive choline transporter. Biochem. Biophys. Res. Commun. 276: 862-867, 2000. 2. Barwick, K. E. S., Wright, J., Al-Turki, S., McEntagart, M. M., Nair, A., Chioza, B., Al-Memar, A., Modarres, H., Reilly, M. M., Dick, K. J., Ruggiero, A. M., Blakely, R. D., Hurles, M. E., Crosby, A. H. Defective presynaptic choline transport underlies hereditary motor neuropathy. Am. J. Hum. Genet. 91: 1103-1107, 2012. 3. Bauche, S., O'Regan, S., Azuma, Y., Laffargue, F., McMacken, G., Sternberg, D., Brochier, G., Buon, C., Bouzidi, N., Topf, A., Lacene, E., Remerand, G., and 30 others. Impaired presynaptic high-affinity choline transporter causes a congenital myasthenic syndrome with episodic apnea. Am. J. Hum. Genet. 99: 753-761, 2016.
    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
    ChT (High Affinity Choline Transporter (ChT))
    Alternative Name
    SLC5A7 (ChT Products)
    Background

    Synonyms: Transcription factor MafA, Pancreatic beta-cell-specific transcriptional activator, RIPE3b1 factor, V-maf musculoaponeurotic fibrosarcoma oncogene homolog A, MAFA

    Tissue Specificity: Preferentially expressed in regulatory T-cells (Tregs).

    Background: The high-affinity choline transporter (ChT) also known as solute carrier family 5 member 7 is a protein in humans that is encoded by the SLC5A7 gene. This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants.

    Molecular Weight
    80 kDa
    Gene ID
    60482
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