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the faster migrating Tg adduct C primarily engages the CaBP1 (zeige S100G ELISA Kits)/P5 oxidoreductase (zeige TXNRD1 ELISA Kits), whereas the slower migrating Tg adduct A primarily engages ERp72 (zeige PDIA4 ELISA Kits).
Present the NMR structure of full-length CaBP1 (zeige S100G ELISA Kits) with Ca(2 (zeige CA2 ELISA Kits)+) bound at the first, third, and fourth EF-hands.
Different kinetics of Ca-dependent binding step between caldendrin and calmodulin (zeige CALM1 ELISA Kits) with AKAP79 (zeige AKAP5 ELISA Kits) suggest their different roles in synaptic function.
We demonstrate that calmodulin (zeige CALM1 ELISA Kits) and caldendrin compete for a partially overlapping binding site on AKAP79 (zeige AKAP5 ELISA Kits) and that their binding is differentially dependent on calcium
CaBP1 (zeige S100G ELISA Kits) regulates voltage-dependent inactivation and activation of Ca(V)1.2 (zeige CACNA1C ELISA Kits) (L-type) calcium channels
Structural basis for the differential effects of CaBP1 (zeige S100G ELISA Kits) and calmodulin (zeige CALM1 ELISA Kits) on Ca(V)1.2 (zeige CACNA1C ELISA Kits) calcium-dependent inactivation.
enhances inactivation, causes a depolarizing shift in the voltage dependence of activation, and does not support Ca2 (zeige CA2 ELISA Kits)+-dependent facilitation of Ca(v)2.1 (zeige CACNA1A ELISA Kits) channels
CaBP1 (zeige S100G ELISA Kits) is able to specifically regulate InsP3 receptor-mediated alterations in [Ca2 (zeige CA2 ELISA Kits)+]i during agonist stimulation.
We describe a new role for CaBP1 (zeige S100G ELISA Kits) in regulation of Ca2 (zeige CA2 ELISA Kits)+ influx through Ca(v)1.2 (zeige CACNA1C ELISA Kits) (L-type) Ca2 (zeige CA2 ELISA Kits)+ channels. CaBP1 (zeige S100G ELISA Kits) interacts directly with the alpha1 subunit of Ca(v)1.2 (zeige CACNA1C ELISA Kits) at sites that also bind Calmodulin (zeige CALM1 ELISA Kits)
the NT and IQ-domains of alpha(1)1.2 mediate functionally distinct interactions with CaBP1 (zeige S100G ELISA Kits) and CaM (zeige CALM1 ELISA Kits) that promote conformational alterations that either stabilize or inhibit inactivation of Ca(v)1.2 (zeige CACNA1C ELISA Kits).
Results show that CaBP1/caldendrin and CaBP2 (zeige CABP2 ELISA Kits) are not required for normal gross retinal and synapse morphology but are necessary for the proper transmission of light responses through the retina; CaBP1/caldendrin and CaBP2 (zeige CABP2 ELISA Kits) likely act by modulating presynaptic Ca(2 (zeige CA2 ELISA Kits)+)-dependent signaling mechanisms.
Study provides the first report of the expression and localization of CaBP1 and caldendrin in the mouse brain
These findings suggest that expression of paracellular tight junction genes is regulated by transcellular CaBP (zeige S100G ELISA Kits) proteins, suggesting that active and passive calcium transport pathways may function cooperatively
TRPV6 (zeige TRPV6 ELISA Kits), NCX1 (zeige SLC8A1 ELISA Kits), and CaBP (zeige S100G ELISA Kits)-9k in the fetal placenta and CaBP (zeige S100G ELISA Kits)-28k in the maternal placenta may play key roles in controlling calcium transport across the placenta during pregnancy.
When immature mice were treated with 17beta-estradiol or progesterone for 3 days, we found that the expressions of Bax (zeige BAX ELISA Kits) and caspase 3 protein (zeige CASP3 ELISA Kits) were increased by estradiol treatment in WT and CaBP (zeige S100G ELISA Kits)-9k KO mice.
our results implicate CaBP1 rather than CaBP4 (zeige CABP4 ELISA Kits) in conferring the anomalous slow inactivation of Ca(v)1.3 (zeige CACNA1D ELISA Kits) Ca(2 (zeige CA2 ELISA Kits)+) currents required for auditory transmission
Regulation of calbindin-D9k (zeige S100G ELISA Kits) expression by 1,25-dihydroxyvitamin D(3) and parathyroid hormone (zeige PTH ELISA Kits) in mouse primary renal tubular cells
These results suggest that the mouse uterine calbindin-D9k (zeige S100G ELISA Kits) gene is expressed under the control of a progesterone response element.
demonstrated that the CaBP (zeige S100G ELISA Kits)-9k is distinctly regulated in the mouse placenta and extra-embryonic membrane, probably via sex steroid hormones (E2 and P4) and their receptors through a complex pathway
Progesterone and its receptor may be dominant factors in the regulation of CaBP (zeige S100G ELISA Kits)-9k but estrogen and ERalpha (zeige ESR1 ELISA Kits) can influence the expression of the CaBP (zeige S100G ELISA Kits)-9k gene via an indirect pathway in the uterus of immature mice.
Calcium binding proteins are an important component of calcium mediated cellular signal transduction. This gene encodes a protein that belongs to a subfamily of calcium binding proteins which share similarity to calmodulin. The protein encoded by this gene regulates the gating of voltage-gated calcium ion channels. This protein inhibits calcium-dependent inactivation and supports calcium-dependent facilitation of ion channels containing voltage-dependent L-type calcium channel subunit alpha-1C. This protein also regulates calcium-dependent activity of inositol 1,4,5-triphosphate receptors, P/Q-type voltage-gated calcium channels, and transient receptor potential channel TRPC5. This gene is predominantly expressed in retina and brain. Alternative splicing results in multiple transcript variants encoding disinct isoforms.
, calcium-binding protein 1
, calcium binding protein 1
, calcium binding protein 5
, calcium binding protein 1 (calbrain)
, S100 calcium-binding protein G
, calbindin 3, (vitamin D-dependent calcium binding protein)
, calbindin D9k
, calbindin-D9K major form
, cytidine 5'-triphosphate synthase 2
, protein S100-G
, vitamin D-dependent calcium-binding protein, intestinal