MYO7A recombinant protein product blog
Tags: Recombinant Protein; MYO7A; Myo7a recombinant protein; Unconventional myosin-VIIa (MYO7A);
The MYO7A myo7a (Catalog #MBS9424072) is a Recombinant Protein produced from E Coli and is intended for research purposes only. The product is available for immediate purchase. The Recombinant Human Unconventional myosin-VIIa (MYO7A), partial reacts with Human and may cross-react with other species as described in the data sheet.The MYO7A myo7a product has the following accession number(s) (GI #189083798) (NCBI Accession #NP_000251.3) (Uniprot Accession #Q13402). 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.
To buy or view more detailed product information and pricing, please click on the technical datasheet page below:
Our knowledge of the role of proteins in cellular processes is continually evolving. Most proteins, including Unconventional myosin-VIIa (MYO7A) 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.
Tag Info: N-terminal 6xHis-SUMO-tagged. Adipose Tissue, Bone, Brain, Connective Tissue, Embryonic Tissue, Eye, Intestine, Nerve, Ovary tissues are correlated with this protein. Abnormalities, Multiple, Congenital Abnormalities, Deafness, Autosomal Dominant 11, Disease Models, Animal, Inflammation, Kidney Diseases, Melanoma, Usher Syndromes, Usher syndrome, type 1B are some of the diseases may be linked to Recombinant Human Unconventional myosin-VIIa (MYO7A), partial. MYO7A also interacts with the following gene(s): CDH23, DFNB31, MYRIP, PCDH15, RAB27A, USH1C, USH1G, VEZT, YY1. The following patways have been known to be associated with this gene.