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SLC38A6 Antibodies
AND SLC38A6 ELISA kits, SLC38A6 Proteins
Many biological assays use antibodies to detect SLC38A6, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC38A6 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC38A6 antibodies...
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SLC38A6 Infographic by Boster Bio
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SLC38A6 Overview
Facts about Probable sodium-coupled neutral amino acid transporter 6.
Probable sodium-coupled neutral amino acid transporter 6 (SLC38A6)
Probable sodium-dependent amino acid/proton antiporter, could be a neuronal transporter for glutamate. .
Gene Information
| Human | |
|---|---|
| Gene Name: | SLC38A6 |
| Uniprot: | Q8IZM9 |
| Entrez: | 145389 |
Family
| Belongs to: |
|---|
| amino acid/polyamine transporter 2 family |
Alternative Names
N system amino acid transporter NAT-1; SNAT6; solute carrier family 38, member 6
Molecular Weight
Mass (kDA):
50.929 kDA
Genomic Context
| Human | |
|---|---|
| Location: | 14q23.1 |
| Sequence: | 14; NC_000014.9 (60981114..61083733) |
Subcellular Localizations
Cell membrane; Multi-pass membrane protein. Colocalizes with synaptotagmins and SNAP25.
Diseases
- Endometrial Polyp
Pathways
- Transport
PTMs
- Acetylation
- Disulfide bond
For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC38A6
bosterbio.com/bosterbio-gene-info-cards/SLC38A6
References
PMID: 12845534 by Mackenzie B., et al. Sodium-coupled neutral amino acid (System N/A) transporters of the SLC38 gene family.
PMID: 28973684 by Biswas P., et al. A mutation in IFT43 causes non-syndromic recessive retinal degeneration.