Thermo Fisher Scientific KCNQ1 Monoclonal Antibody (N37A/10), APC
KCNQ1 단백질을 인식하는 마우스 모노클로날 항체로, APC 형광 표지되어 있습니다. Western blot, IHC, ICC, IP 등 다양한 응용에 적합합니다. 인간, 생쥐, 햄스터, 랫트 시료에 반응하며, 단백질 G 정제 및 4°C 보관이 권장됩니다.
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Applications and Tested Dilutions
| Application | Tested Dilution | Notes |
|---|---|---|
| Western Blot (WB) | 1:1,000 | |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:1,000 | |
| Immunohistochemistry (PFA fixed) (IHC (PFA)) | 1:1,000 | |
| Immunocytochemistry (ICC/IF) | 1:100 | |
| Immunoprecipitation (IP) | Assay-dependent | |
| Antibody Microarray (AM) | Assay-dependent |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Hamster, Human, Mouse, Rat |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | N37A/10 |
| Immunogen | Fusion protein amino acids 2–101 of human KCNQ1 |
| Conjugate | APC (Allophycocyanin) |
| Excitation/Emission Max | 651 / 660 nm |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein G |
| Storage Buffer | 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA |
| Contains | No preservative |
| Storage Conditions | 4°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2931861 |
Available Formats
- Unconjugated (MA5-27676)
- FITC (MA5-45408)
- PE (MA5-45410)
- PerCP (MA5-45409)
- Custom conjugation available upon request
Product Specific Information
1 µg/mL of MA5-45407 was sufficient for detection of KCNQ1 in 10 µg of COS-1 cell lysate transiently expressing KCNQ1 by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
Detects approximately 75 kDa.
Target Information
Voltage-gated K⁺ channels in the plasma membrane control repolarization and the frequency of action potentials in neurons, muscles, and other excitable cells.
KCNQ1, in complex with KCNE1, is expressed mainly in the heart and cochlea and regulates the slow depolarization-activated potassium current.
Mutations in KCNQ1 or KCNE1 can lead to cardiac disease, while KCNQ4 mutations are linked to deafness.
KCNQ proteins, including KCNQ1 and KCNQ4, have six transmembrane domains and function as tetramers.
KCNQ4 forms heteromeric channels with KCNQ3 and is expressed in several tissues, including cochlear outer hair cells.
For Research Use Only.
Not for use in diagnostic procedures. Not for resale without express authorization.
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