|Datasheet||Specific References||Reviews||Related Products||Protocols|
|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive ,Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
A polyhistidine-tag is an amino acid motif in proteins that consists of at least five histidine (His) residues, often at the N- or C-terminus of the protein.
Polyhistidine-tags are often used for affinity purification of polyhistidine-tagged recombinant proteins expressed in Escherichia coli and other prokarfyotic expression systems.
|Mouse OSTM1 ORF mammalian expression plasmid, C-GFPSpark tag||MG51952-ACG|
|Mouse OSTM1 ORF mammalian expression plasmid, C-OFPSpark / RFP tag||MG51952-ACR|
|Mouse OSTM1 ORF mammalian expression plasmid, C-Flag tag||MG51952-CF|
|Mouse OSTM1 ORF mammalian expression plasmid, C-His tag||MG51952-CH|
|Mouse OSTM1 ORF mammalian expression plasmid, C-Myc tag||MG51952-CM|
|Mouse OSTM1 ORF mammalian expression plasmid, C-HA tag||MG51952-CY|
|Mouse OSTM1 Gene cDNA clone plasmid||MG51952-G|
|Mouse OSTM1 ORF mammalian expression plasmid, N-Flag tag||MG51952-NF|
|Mouse OSTM1 ORF mammalian expression plasmid, N-His tag||MG51952-NH|
|Mouse OSTM1 ORF mammalian expression plasmid, N-Myc tag||MG51952-NM|
|Mouse OSTM1 ORF mammalian expression plasmid, N-HA tag||MG51952-NY|
|Mouse OSTM1 natural ORF mammalian expression plasmid||MG51952-UT|
|Learn more about expression Vectors|
Osteopetrosis-associated transmembrane protein 1 (OSTM1) is a Single-pass type I membrane protein. It is expressed in many hematopoietic cells of the myeloid and lymphoid B- and T-lineages. The analysis of OSTM1 association with CLCN7 demonstrated that OSTM1 requires CLCN7 to localize to lysosomes, whereas the formation of a CLCN7-OSTM1 complex is required to stabilize CLCN7. The researches found that OSTM1 plays a major role in myelopoiesis and lymphopoiesis and provided evidence of a crosstalk mechanism between hematopoietic cells for osteoclast activation. Thus, OSTM1 has a important role in osteoclast function and activation. The loss of function of OSTM1 results in deregulation of multiple hematopoietic lineages in addition to osteoclast lineage, OSTM1-defect patients display the most severe recessive osteopetrotic phenotype and die at early ages. Furthermore, it is suggested that OSTM1 has a primary role in neural development not related to lysosomal dysfunction. The canonical Wnt/beta-catenin signaling pathway may be a molecular basis for OSTM1 mutations and severe autosomal recessive osteopetrosis (ARO).
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3. Lange, PF. et al., 2006, Nature. 440 (7081): 220-223
4. Maranda, B. et al., 2008, J Bone Miner Res. 23 (2): 296-300.
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6. Pata, M.et al., 2008, J Biol Chem. 283 (45): 30522-30530.