
Thermo Fisher Scientific SCN9A Polyclonal Antibody
SCN9A 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot에 최적화되어 있습니다. 인간 및 생쥐 시료에 반응하며, Affinity chromatography로 정제되었습니다. 액상 형태로 제공되며, -20°C에서 보관합니다.
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Applications
Western Blot (WB)
- Tested Dilution: 1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human SCN9A (Accession Q15858), corresponding to amino acid residues T660–C710 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2903293 |
Product Specific Information
Antibody detects endogenous levels of total Nav1.7.
Target Information
Epithelial sodium channels (ENaC) are amiloride-sensitive ion channels belonging to the Degenerin/epithelial sodium channel (Deg/ENaC) superfamily. These channels share structural similarity with two short intracellular termini, two transmembrane segments, and a large extracellular loop containing a conserved cysteine-rich region. ENaC has three homologous isoforms (α, β, γ) and plays a critical role in sodium and fluid balance across epithelial tissues such as kidney, lung, and colon. It mediates aldosterone-dependent sodium reabsorption in the distal nephron, regulating blood pressure. ENaC activity is modulated partly through interaction with the CFTR chloride channel. Gain-of-function mutations in β- or γ-ENaC can cause Liddle’s syndrome (hypertension), while loss-of-function mutations in α- or β-ENaC lead to pseudohypoaldosteronism type 1 (PHA-1).
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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