Thermo Fisher Scientific SLC6A15 Polyclonal Antibody
SLC6A15 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot 및 Immunoprecipitation에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 1 mg/mL 농도의 액상 형태입니다. 인간 시료에 반응하며, 4°C에서 보관합니다.
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Applications
Western Blot (WB)
- Tested Dilution: 1:2,000–1:10,000
Immunoprecipitation (IP)
- Tested Dilution: 2–10 µg/mg lysate
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Region between residue 650–700 of Human Solute Carrier Family 6 (neutral amino acid transporter), Member 15 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | Phosphate/Tris citrate, pH 7–8 |
| Contains | 0.09% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Wet ice |
Product Specific Information
The recommended shelf life for this product is 1 year from date of receipt.
Target Information
SLC6A15 (solute carrier family 6, neutral amino acid transporter, member 15), also known as sodium-dependent neutral amino acid transporter B(0)AT2, transporter v7-3, NTT73, or SBAT1, is a 730 amino acid multi-pass membrane protein functioning as a sodium-dependent neutral amino acid transporter.
It belongs to the sodium neurotransmitter symporter (SNF) family and SLC6A15 subfamily, differing from other members in that it is not chloride-dependent.
SLC6A15 is expressed in the brain and encoded by a gene located on human chromosome 12, which contains over 1,100 genes (~4.5% of the human genome).
Chromosome 12 is linked to various disorders including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p, which causes facial developmental defects and seizure disorders.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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