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SLC17A8
Enables L-glutamate transmembrane transporter activity. Acts upstream of or within L-glutamate transmembrane transport. Located in synaptic vesicle membrane. Is integral component of synaptic vesicle membrane. Is expressed in brain; cochlear ganglion; and sensory organ. Used to study autosomal dominant nonsyndromic deafness 25. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 25. Orthologous to human SLC17A8 (solute carrier family 17 member 8).
Protein class
Disease related genes, Human disease related genes, Metabolic proteins, Potential drug targets, Transporters
Predicted location
Membrane
Single cell type specificity
Group enriched (Proximal enterocytes, Endometrial ciliated cells)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Not detected
More Types Infomation
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- Species Reactivity: Human
- Type: Mouse antibody
- Application: ELISA, WB
- Rabbit Anti-Slc17a8 Recombinant Antibody (clone rN34/34.2) (VS-0422-LC109)
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- Species Reactivity: Rat, T. californica, Mouse
- Type: Rabbit IgG
- Application: ICC, WB, IF
- Rat Anti-Slc17a8 Recombinant Antibody (clone rtN34/34.2) (VS-0422-LC108)
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- Species Reactivity: Rat, T. californica, Mouse
- Type: Rat IgG2b
- Application: ICC, WB, IF
- Mouse Anti-Slc17a8 Recombinant Antibody (clone mN34/34.2) (VS-0422-LC107)
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- Species Reactivity: Rat, T. californica, Mouse
- Type: Mouse IgG2a
- Application: ICC, WB, IF
- Rabbit Anti-SLC17A8 Recombinant Antibody (VS-0223-WK89) (VS-0223-WK89)
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- Derivation: Rabbit
- Species Reactivity: Rat, Mouse
- Type: Rabbit IgG
- Application: IHC, IHC-P
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For Research Use Only. Not For Clinical Use.