Description
| Clone | IHC506 |
| Source/Clonality | Mouse Monoclonal |
| Positive Control | Appendix, Uterus, Vessel Wall |
| Dilution Range | 1:200 |
Actin is part of the cytoskeletal system of all cell types. Smooth Muscle Actin is found in myofibroblasts and myoepithelium, but not in cardiac and skeletal muscles. Labelling of smooth muscle actin in concert with muscle specific actin staining can allow for differentiation between rhabdomyosarcoma and leiomyosarcoma, as Muscle specific actin is found in rhabdomyoblasts, while smooth muscle actin is found in leiomyosarcomas.
| Clone | IHC506 |
| Source/Clonality | Mouse Monoclonal |
| Positive Control | Appendix, Uterus, Vessel Wall |
| Dilution Range | 1:200 |
K-PANOPA
SKU: 700004323
100 assays (manual) / 1000 assays (microplate) / 1100 assays (auto-analyser)
| Content: | 100 assays (manual) / 1000 assays (microplate) / 1100 assays (auto-analyser) |
| Shipping Temperature: | Ambient |
| Storage Temperature: | Short term stability: 2-8oC, Long term stability: See individual component labels |
| Stability: | > 2 years under recommended storage conditions |
| Analyte: | Nitrogen, Primary Amino Nitrogen, YAN |
| Assay Format: | Spectrophotometer, Microplate, Auto-analyser |
| Detection Method: | Absorbance |
| Wavelength (nm): | 340 |
| Signal Response: | Increase |
| Linear Range: | 0.2 to 10 µg of amino nitrogen per assay |
| Limit of Detection: | 2.59 mg N/L |
| Reaction Time (min): | ~ 15 min |
| Application examples: | Grape juice, must, wine and other materials. |
| Method recognition: | Novel method |
The Primary Amino Nitrogen (PANOPA) Assay Kit is suitable for the measurement and analysis of primary amino nitrogen in grape juice/must and wine.
Note for Content: The number of manual tests per kit can be doubled if all volumes are halved. This can be readily accommodated using the MegaQuantTM Wave Spectrophotometer (D-MQWAVE).
Display our complete list of nitrogen test kits.
View White paper – Free Amino Nitrogen.
Advantages
The Primary Amino Nitrogen (PANOPA) Assay Kit is suitable for the measurement and analysis of primary amino nitrogen in grape juice/must and wine.
TGW16 Technical Parameter：
| Max. Speed | 16000rpm |
| Max. RCF | 19040×g |
| Max. Capacity | 10×5ml |
| Time Range | 0~99min59s |
| RPM/RCF Convert | Yes |
| Noise (dB) | ≤ 55 |
| Acc/Dec | 10 Kinds |
| Speed Accuracy | ±20r/min |
| Voltage(V/Hz) | AC 220V/110V 50HZ/60HZ |
| Size (W x D x Hmm) | 355×270×205mm |
| Net Weight(Kg) | 16KG |
| Certificates | CE,ISO & Calibration report are available |
Matched Rotors for TGW16
| Order No | Rotor | Max speed (rpm) | Max Volume(ml) | Max RCF (g) |
| W16-1 | Angle rotor | 16000 | 40×0.2ml | 19040 |
| W16-2 | Angle Rotor | 16000 | 24×0.5ml | 18480 |
| W16-3 | Angle Rotor | 16000 | 12×1.5/2ml | 17940 |
| W16-4 | Angle Rotor | 16000 | 10x5ml | 17880 |
| W16-5 | Angle Rotor | 14000 | 20×1.5/2ml | 15580 |
| W16-6 | Angle Rotor | 14000 | 4x8PCR | 12070 |
1. Brushless motor, no pollution, free-maintenane.
2. Microprocessor control, LCD display which indicates the speed, time, RCF in operation, 10 kinds of brake setting , operate simply.
3. Electric lid lock, super speed, imbalance protection.
4. The centrifuge body is made of high quality steel, stainless steel chamber, safe and reliable.
5. Rotor is connected to spindle by specialized taper sleeve, loading simple and quick, no direction.
6. 3 tiers protection steel cover and get the ideal centrifuation result.
Interested in the analysis of DNA or RNA modifications? Then this DNA polymerase could help to analyze such modifications. The m6A sensitive DNA polymerase exhibits increased misincorporation rates opposite m6A, while unmodified adenine is not affected. This prevents the loss of methylation information during reverse transcription and thus allows direct m6A sequencing. For further information refer to the original publication.
Available upon request and for R&D use only – Contact Us
The m6A sensitive DNA polymerase is supplied as a 5 µM solution containing glycerol and is supplied together with 10x reaction buffer.
The enzyme can also be used for real-time cycling, when adding a suitable dye.
Interested in the analysis of DNA or RNA modifications? Then this DNA polymerase could help to analyze such modifications. The m6A sensitive DNA polymerase exhibits increased misincorporation rates opposite m6A, while unmodified adenine is not affected. This prevents the loss of methylation information during reverse transcription and thus allows direct m6A sequencing. For further information refer to the original publication.