|The MYL2 myl2 (Catalog #MBS952509) is a Recombinant Protein produced from E Coli or Yeast or Baculovirus or Mammalian Cell and is intended for research purposes only. The product is available for immediate purchase.
The MYL2 myl2 product has the following accession number(s) (GI #94981553) (NCBI Accession #NP_000423.2) (Uniprot Accession #P10916). Researchers may be interested in using Bioinformatics databases such as those available at The National Center for Biotechnology Information (NCBI) website for more information about accession numbers and the proteins they represent. Even researchers unfamiliar with bioinformatics databases will find the NCBI databases to be quite user friendly and useful. The amino acid sequence is listed below:
APKKAKKRAG GANSNVFSMF EQTQIQEFKE AFTIMDQNRD GFIDKNDLRD TFAALGRVNV KNEEIDEMIK EAPGPINFTV FLTMFGEKLK GADPEETILN AFKVFDPEGK GVLKADYVRE MLTTQAERFS KEEVDQMFAA FPPDVTGNLD YKNLVHIITH GEEKD.
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Our knowledge of the role of proteins in cellular processes is continually evolving. Most proteins, including Myosin regulatory light chain 2, ventricular/cardiac muscle isoform (MYL2) are typically involved in one or more signaling pathways or biological processes. Professionally manufactured recombinant proteins are increasingly becoming essential and commonplace tools for elucidating new knowledge about the role of proteins in both health and disease.
Species: Human. Storage Buffer: Tris-based buffer, 50% glycerol
Tag Information: Tag type will be determined during the manufacturing process. Cardiomegaly, Cardiomyopathy, Familial Hypertrophic, 10, Cardiomyopathy, Hypertrophic, Cardiomyopathy, Hypertrophic, Familial, Cardiovascular Diseases, Heart Diseases, Hypertension, Hypertrophy, Inflammation, Neoplasms are some of the diseases may be linked to Recombinant Human Myosin regulatory light chain 2, ventricular/cardiac muscle isoform (MYL2). Bone, Embryonic Tissue, Eye, Heart, Lung, Lymph Node, Mouth, Muscle, Nerve, Vascular tissues are correlated with this protein. MYL2 also interacts with the following gene(s): MYBPC3, MYH7, MYL3, TNNI3, TNNT2, TPM1, TTN. The following patways have been known to be associated with this gene.