![]() Find out everything there's to know about Zoombak employees. All you have to do is type in a couple of keywords and we'll bring you the exact information you wanted!ġ4 Zoombak employees in database. ![]() ![]() With our employee database, the possibilities are endless. Learn about salaries, pros and cons of working for Zoombak directly from the past employees.įind People by Employers You can rekindle an old relationship, reconnect with a long-lost friend, former boss, business acquaintance who might be useful in your new line of work. ![]() You can even request information on how much does Zoombak pay if you want to. You can filter them based on skills, years of employment, job, education, department, and prior employment. Zoombak List of Employees There's an exhaustive list of past and present employees! Get comprehensive information on the number of employees at Zoombak. Founder: Simon Buckingham Founded: 2006 Headquarters: New York City, NY Defunct: 2011 Parent organizations: BrickHouse Security, Liberty Media Corporation acquired Zoombak, LLC from TruePosition, Inc., a subsidiary of Liberty Media. It used satellite-enabled GPS and a location network server for tracking. However, in a minority of KG1B cells, CD164 is more prominently expressed at the plasma membrane and in the recycling endosomes, suggesting that its distribution is regulated in cells of hematopoietic origin.Zoombak Inc was a U.S.-based company which developed GPS tracking devices for people and items. By confocal microscopy, human CD164 in CD34 +CD38 +hematopoietic progenitor (KG1B) and epithelial cell lines appears to be localized primarily in endosomes and lysosomes, with low concentrations at the cell surface. Whereas the human CD164 gene is located on chromosome 6q21, the mouse gene occurs in a syntenic region on chromosome 10B1–B2. Comparative analysis of murine MGC-24v/CD164(E1–6) with human CD164(E1–6) revealed two potential splice variants and a similar genomic structure. This study provides additional evidence that human CD164(E1–6) represents the ortholog of murine MGC-24v and rat endolyn. Three human CD164(E1–6) mRNA species, exhibiting differential polyadenylation site usage, are differentially expressed in hematopoietic and non-hematopoietic tissues. The 103B2/9E10 and 105A5 epitopes, which specify ligand binding characteristics, are located on the exon 1-encoded mucin domain I. The predominant CD164(E1–6) isoform, encoded by six exons, is a type I transmembrane protein containing two extracellular mucin domains (I and II) interrupted by a cysteine-rich non-mucin domain. We have identified three novel human CD164 variants derived by alternative splicing of bona fide exons from a single genomic transcription unit. Functional analyses have indicated that the human CD164 sialomucin may play a key role in hematopoiesis by facilitating the adhesion of human CD34 +cells to the stroma and by negatively regulating CD34 +CD38 lo/− cell proliferation.
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