SCN4B Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- Target See all SCN4B Proteins
- SCN4B (Sodium Channel, Voltage-Gated, Type IV, beta Subunit (SCN4B))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This SCN4B protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human SCN4B (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product SCN4B Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- SCN4B (Sodium Channel, Voltage-Gated, Type IV, beta Subunit (SCN4B))
- Alternative Name
- Scn4b (SCN4B Products)
- Synonyms
- LQT10 Protein, Navbeta4 Protein, Gm1471 Protein, sb:cb973 Protein, scn4b.2 Protein, si:ch211-139a5.5 Protein, scn4b.1 Protein, scn4b1 Protein, zgc:165389 Protein, sodium voltage-gated channel beta subunit 4 Protein, sodium channel, type IV, beta Protein, sodium channel, voltage-gated, type IV, beta b Protein, sodium channel, voltage-gated, type IV, beta a Protein, SCN4B Protein, Scn4b Protein, scn4bb Protein, scn4ba Protein
- Background
- The protein encoded by this gene is one of several sodium channel beta subunits. These subunits interact with voltage-gated alpha subunits to change sodium channel kinetics. The encoded transmembrane protein forms interchain disulfide bonds with SCN2A. Defects in this gene are a cause of long QT syndrome type 10 (LQT10). Three protein-coding and one non-coding transcript variant have been found for this gene.[provided by RefSeq, Mar 2009].
- Molecular Weight
- 22 kDa
- NCBI Accession
- NP_777594
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