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these data suggest that Adrm1 (zeige Adrm1 ELISA Kits), a new Atp6v0d2-interacting protein, plays an important role in osteoclast differentiation, and in particular the fusion of preosteoclasts.
High V-ATPase (zeige ATP6V1H ELISA Kits) expression is associated with Bone Pain Induced by Multiple Myeloma.
we propose that PTH (zeige PTH ELISA Kits) has a direct effect on osteoblasts and osteoclasts, and that this effect is mediated through PTH1R (zeige PTH1R ELISA Kits), thus contributing to bone remodeling
Insulin (zeige INS ELISA Kits) significantly activated ERK1/2 (zeige MAPK1/3 ELISA Kits) MAP kinase (zeige MAPK1 ELISA Kits) as well as markedly induced the expression of NFATc1 (zeige NFATC1 ELISA Kits), an osteoclast marker gene, and Atp6v0d2, an osteoclast fusion-related gene.
V-ATPase (zeige ATP6V1H ELISA Kits) has a role in modulating a macrophage phenotype towards tumor-associated macrophages through the action of the a2 isoform of V-ATPase (zeige ATP6V1H ELISA Kits)
Luteolin can be effective in reducing bone resorption and that this effect of luteolin may be through disruption of osteoclast V-ATPase a3 (zeige TCIRG1 ELISA Kits)-d2 interaction.
PKCdelta (zeige PKCd ELISA Kits) deficiency does not perturb formation of the ruffled border or trafficking of lysosomal vesicles containing the vacuolar-ATPase (v-ATPase (zeige DNAH8 ELISA Kits)).
these findings suggest that the critical role of ATP6v0d2 may be limited to the control of bone homeostasis under normal development.
The data indicate that integrity of lipid rafts regulates the activity of V-ATPase (zeige ATP6V1H ELISA Kits) in osteoclasts, suggesting that cholesterol-lowering agents might be useful for inhibiting osteoclast-dependent bone resorption.
Atp6v0d2 is a regulator of osteoclast fusion and bone formation.
Data indicate for the first time that the NFATc1 (zeige NFATC1 ELISA Kits)/Atp6v0d2 and DC-STAMP (zeige TM7SF4 ELISA Kits) signaling axis plays a key role in the osteoclast multinucleation process, which is essential for efficient bone resorption.
Total VHA-A transcript and protein, together with levels of the truncated variant, were induced by copper. The absence of a genomic sequence representing the truncated variant suggests a RNA editing event causing the production of the truncated VHA-A.
oxidative inhibition was unaffected in plants expressing VHA-A C279S and VHA-A C535S, indicating that disulfide bridges involving these cysteine residues are not essential for oxidative inhibition
Subunit of the integral membrane V0 complex of vacuolar ATPase. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system (By similarity). May play a role in coupling of proton transport and ATP hydrolysis. Regulator of osteoclast fusion and bone formation.
V-ATPase subunit d 2
, V-type proton ATPase subunit d 2
, vacuolar proton pump subunit d 2
, ATPase, H+ transporting, V0 subunit D
, osteoclast-specific vacuolar ATP synthase
, vacuolar proton-translocating ATPase d subunit d2
, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2
, ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d
, Vacuolar proton pump subunit d 2
, V-type H+-ATPase
, vacuolar ATPase 69 kDa subunit
, ATPase, H+ transporting, lysosomal V0 subunit D2