IgG4 Protein (AA 99-327) (His tag)
Kurzübersicht für IgG4 Protein (AA 99-327) (His tag) (ABIN7668933)
Target
Protein-Typ
Spezies
Quelle
Applikation
Reinheit
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Proteineigenschaft
- AA 99-327
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Aufreinigungstag / Konjugat
- Dieses IgG4 Protein ist gelabelt mit His tag.
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Verwendungszweck
- Recombinant Human IgG4-Fc Protein (His Tag)
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Sequenz
- Glu99-Lys327
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Aufreinigung
- > 95 % as determined by reducing SDS-PAGE.
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Sterilität
- 0.2 μm filtered
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Endotoxin-Niveau
- < 1.0 EU/mg of the protein as determined by the LAL method
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Biological Activity Comment
- Not validated for activity
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.
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Buffer
- Lyophilized from a 0.2 μm filtered solution in PBS with 5 % Trehalose and 5 % Mannitol.
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Lagerung
- 4 °C,-20 °C,-80 °C
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Informationen zur Lagerung
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
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Haltbarkeit
- 12 months
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- IgG4
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Substanzklasse
- Antibody
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Hintergrund
- IGHG4,Ig gamma-4 chain C region,IgG4 Fc,SCN3B (sodium channel, voltage-gated, type III, beta,human IgG1-Fc chimera) belongs to the sodium channel auxiliary subunit SCN3B family. It contains 1 Ig-like C2-type (immunoglobulin-like) domain. Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. SCN3B gene encodes one member of the sodium channel beta subunit gene family, and influences the inactivation kinetics of the sodium channel. Two alternatively spliced variants, encoding the same protein, have been identified. Defects in SCN3B are the cause of Brugada syndrome type 7. A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram. It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs (called ventricular fibrillation), the individual will faint and may die in a few minutes if the heart is not reset.
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Molekulargewicht
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Calculated MW: 25.1 kDa
Observed MW: 35 kDa
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UniProt
- P01861
Target
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