ChT anticorps (AA 446-580)
Aperçu rapide pour ChT anticorps (AA 446-580) (ABIN7997529)
Antigène
Voir toutes ChT AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
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Épitope
- AA 446-580
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Fonction
- Anti-SLC5A7 Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Anti-SLC5A7 Antibody. Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human SLC5A7 recombinant protein (Position: R446-Q580).
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Isotype
- IgG
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Indications d'application
- 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
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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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. -
Date de péremption
- 12 months
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- ChT (High Affinity Choline Transporter (ChT))
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Autre désignation
- SLC5A7
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Sujet
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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.
Gene Full Name: solute carrier family 5 member 7
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Poids moléculaire
- 80 kDa
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ID gène
- 60482
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UniProt
- Q9GZV3
Antigène
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