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OSTM1 encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. Additionally we are shipping OSTM1 Proteins (7) and OSTM1 Kits (2) and many more products for this protein.
Showing 10 out of 43 products:
Human Monoclonal OSTM1 Primary Antibody for ELISA - ABIN1997769
Chalhoub, Benachenhou, Rajapurohitam, Pata, Ferron, Frattini, Villa, Vacher: Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. in Nature medicine 2003
Show all 2 references for ABIN1997769
Human Monoclonal OSTM1 Primary Antibody for ELISA - ABIN1997767
Lange, Wartosch, Jentsch, Fuhrmann: ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function. in Nature 2006
Show all 2 references for ABIN1997767
KIF5B (show KIF5B Antibodies) is essential for Ostm1 intracellular dispersion.
Ostm1 has a primary and autonomous role in neuronal homeostasis
Common gating underlies the slow voltage activation of ClC-7 (show CLCN7 Antibodies).
we describe for the first time homozygous microdeletions of different sizes affecting the OSTM1 gene in two unrelated consanguineous families with children suffering from neuronopathic infantile malignant osteopetrosi
The authors show that both the aminoterminus and transmembrane span of the Ostm1 beta-subunit (show POLG Antibodies) are required for ClC-7 (show CLCN7 Antibodies) Cl(-)/H(+)-exchange, whereas the Ostm1 transmembrane domain suffices for its ClC-7 (show CLCN7 Antibodies)-dependent trafficking to lysosomes.
mutation in the human GL gene leads to severe recessive osteopetros (show CSF1 Antibodies)is
The human GIPN gene has 6 exons and 5 introns, and encodes a 334-aa protein.
A novel mutation affecting the OSTM1 locus responsible for ARO (show CYP19A1 Antibodies). In addition to common clinical features of osteopetrosis (show CSF1 Antibodies), the patient developed a unique neuronal pathology that provided evidence for the role of OSTM1 in normal neuronal cell development.
This study reports on a 12-month-old female with recessive OSMT1 mutations and neuroimaging findings suggesting a malignant infantile osteopetrosis (show CSF1 Antibodies).
mutations in OSTM1 such as the C-terminal deletion mutant studied herein provoke dysregulation of the canonical Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway, providing a molecular basis for severe autosomal recessive osteopetrosis (show CSF1 Antibodies)
Truncated OSTM1 significantly inhibited the expression of osteoclast marker genes through the down-regulation of the BLIMP1 (show PRDM1 Antibodies)-NFATc1 (show NFATC1 Antibodies) axis.
Our in vivo structure-function analysis of ClC-7 (show CLCN7 Antibodies) reveals that both protein-protein interactions and ion transport must be considered in the pathogenesis of ClC-7 (show CLCN7 Antibodies)-related diseases.
Omi (show HTRA2 Antibodies) is a recessive mutation in the Ostm1 gene affecting teeth and coat color.
Ostm1 is a bona fide target of miR (show MLXIP Antibodies)-140, which is significantly decreased during adipogenic differentiation.
Neuropathologic changes similar to neuronal ceroid lipofuscinosis (show CLN6 Antibodies) are found in osteoporosis associated transmembrane protein 1 (show TMEM1 Antibodies) (Ostml)-deficient mice.
mutation induces severe malignant autosomal recessive osteopetrosis (show CSF1 Antibodies); studies show that Gl protein function is absolutely required for osteoclast and melanocyte maturation and function
both ClC-7 (show CLCN7 Antibodies) and Ostm1 proteins co-localize in late endosomes and lysosomes of various tissues, as well as in the ruffled border of bone-resorbing osteoclasts
microphthalmia transcription factor (show MITF Antibodies) regulates Clcn7 and Ostm1 expression in osteoclasts
This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.
osteopetrosis-associated transmembrane protein 1
, osteopetrosis associated transmembrane protein 1
, GAIP-interacting protein N terminus
, chloride channel 7 beta subunit
, grey-lethal osteopetrosis
, grey lethal osteopetrosis
, GAIP interacting protein N terminus
, osteopetrosis associated transmembrane protein 1-like