MYL12A, Recombinant, His-Tag (Myosin Regulatory Light Chain 12A, MLC-2B, Myosin RLC, Myosin Regulatory Light Chain 2, Nonsarcomeric, Myosin Regulatory Light Chain MRLC3, MLCB, MRLC3, RLC)
Catalog No : USB-138167
583.92€
0.00€
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| Product name | MYL12A, Recombinant, His-Tag (Myosin Regulatory Light Chain 12A, MLC-2B, Myosin RLC, Myosin Regulatory Light Chain 2, Nonsarcomeric, Myosin Regulatory Light Chain MRLC3, MLCB, MRLC3, RLC) | ||
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| Catalog No | USB-138167 | ||
| Supplier’s Catalog No | 138167 | ||
| Supplier | US Biologicals | ||
| Source antigen | Recombinant, E.coli | ||
| Reactivity | |||
| Cross reactivity | |||
| Applications | |||
| Molecular weight | 22.4 | ||
| Storage | -20°C | ||
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| Other names | |||
| Grade | Highly Purified | ||
| Purity | ~90% (SDS-PAGE) | ||
| Form | Supplied as a liquid in 20mM Tris-HCl, pH 8.0, 1mM DTT, 20% glycerol. | ||
| Reactivity life | 6 months | ||
| Note | For reserch purpose only | ||
| Purity | ~90% (SDS-PAGE) | ||
| Description | MYL12A, also known as myosin regulatory light chain 12A, plays an important role in regulation of both smooth muscle and nonmuscle cell contractile activity via its phosphorylation. This protein is implicated in cytokinesis, receptor capping, and cell locomotion. Recombinant human MYL12A protein, fused to His-tag at N-terminal domain, was expressed in E.coli and purified by using conventional chromatography. Source: Recombinant protein corresponding to aa1-171 from human MYL12A, fused to His-tag at N-terminal domain, expressed in E.coli. Molecular Weight: ~22.4kD (MALDI-TOF) AA Sequence: MGSSHHHHHH SSGLVPRGSH MGSHMSSKRT KTKTKKRPQR ATSNVFAMFD QSQIQEFKEA FNMIDQNRDG FIDKEDLHDM LASLGKNPTD EYLDAMMNEA PGPINFTMFL TMFGEKLNGT DPEDVIRNAF ACFDEEATGT IQEDYLRELL TTMGDRFTDE EVDELYREAP IDKKGNFNYI EFTRILKHGA KDKDD Storage and Stability: May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. | ||
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