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ChT antibody (AA 446-580)

This Rabbit Polyclonal antibody specifically detects ChT in WB, FACS and ELISA. It exhibits reactivity toward Mouse, Human and Rat.
Catalog No. ABIN7601754

Quick Overview for ChT antibody (AA 446-580) (ABIN7601754)

Target

See all ChT Antibodies
ChT (High Affinity Choline Transporter (ChT))

Reactivity

  • 10
  • 10
  • 10
  • 9
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Mouse, Human, Rat

Host

  • 11
  • 10
Rabbit

Clonality

  • 11
  • 10
Polyclonal

Conjugate

  • 15
  • 2
  • 2
  • 2
This ChT antibody is un-conjugated

Application

  • 12
  • 8
  • 7
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), ELISA
  • Binding Specificity

    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 446-580

    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
  • 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

    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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