|Datasheet||Specific References||Reviews||Related Products||Protocols|
|ORF Clone of sodium channel, voltage-gated, type III, beta DNA.|
|HSA243396, SCNB3, SCN3B|
|Identical with the Gene Bank Ref. ID sequence.|
|Whatman FTA elute card (Cat: WB120410) contains 5-10 μg of plasmid.|
|The Whatman FTA elute card can be stored at room temperature for three months under dry condition.|
The pGEM-T is 3kb in length, and contains the amplicin resistance gene, conferring selection of the plasmid in E. coli, and the ori site which is the bacterial origin of replication. The plasmid has multiple cloning sites as shown below. The coding sequence was inserted by TA cloning. Many E. coli strains are suitable for the propagation of this vector including JM109, DH5α and TOP10.
The coding sequence can be easily obtained by digesting the vector with proper restriction enzyme(s). The coding sequence can also be amplified by PCR with M13 primers, or primer pair SP6 and T7.
|Human SCN3B Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG13897-G-F|
|Human SCN3B Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG13897-G-H|
|Human SCN3B Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG13897-G-M|
|Human SCN3B Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG13897-G-N|
|Human SCN3B Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG13897-G-Y|
|Product name||Product name|
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.