FKBP1B Antibody, HRP conjugated

1. Our FRET-based HTS detects RyR binding of accessory proteins calmodulin (CaM) or FKBP12.6...One compound increased FRET and inhibited RyR1, which was only significant at nM [Ca(2+)], and accentuated without CaM present. PMID: 27760856
2. Total chemical synthesis, refolding, and crystallographic structure of fully active immunophilin calstabin 2 PMID: 27670942
3. results suggest that both FKBP12.6 and FKBP12 play critical roles in regulating RyR2 function by facilitating the termination of SOICR. PMID: 27154203
4. Sirolimus-FKBP12.6 impairs endothelial barrier function by activation of protein kinase C-alpha and downstream disruption of the p120-VE cadherin interaction in vascular endothelium. PMID: 23887639
5. FKBP12.6-deficient mice with cardiac hypertrophy do not display exercise-induced arrhythmia and/or sudden cardiac death. PMID: 22087651
6. analysis of the ryanodine receptor FK506-binding protein subunit PMID: 20404344
7. Characterize the kinetics of FKBP12/12.6 binding to RyR2 in ventricular myocytes and effects on calcium signaling. PMID: 20431056
8. localization of binding site to the NH2-terminal domain of the cardiac Ca2+ release channel PMID: 12446682
9. Data show that VTSIP- and ARVD2-associated point mutations influence positively and negatively, respectively, the binding of RyR2 to its gating protein FKBP12.6. PMID: 12459180
10. data demonstrate that defective regulation of ryanodine receptor 2 causes altered cellular phenotype via profound perturbations in intracellular calcium signaling and highlight a key modulatory role of FK506 binding protein 12.6 PMID: 12754204
11. FKBP1B gene is involved in the genetic susceptibility to the AITDs development in the studied family. PMID: 15497458
12. novel interaction site for FKBP12.6 may be present at the RyR2 C terminus, proximal to the channel pore, a sterically appropriate location that would enable this protein to play a central role in the modulation of this critical ion channel PMID: 15591045
13. FKBP12.6 plays a critical role in Ca channel gating, the R2401H mutation can be expected to alter Ca-induced Ca release and E-C coupling resulting in CPVT. PMID: 15749201
14. Enhancing calstabin binding to ryanodine receptors improves cardiac and skeletal muscle function in heart failure. PMID: 15972811
15. the redox state of the RyR is intimately connected with FKBP binding affinity. PMID: 17200109
16. Data show that K201 abolished spontaneous calcium release in cardiac myocytes, and that treating ventricular myocytes with FK506 to dissociate FKBP12.6 from ryanodine receptor RyR2 did not affect the suppression of spontaneous Ca2+ release by K201. PMID: 17313373
17. Results describe abrupt changes in the expression of FKBP12.6, SERCA2a, PKA, and ECE on reperfusion against ischemia, which are responsible for the rapid occurrence of ventricular fibrillation, and their prevention by CPU86017. PMID: 17506935
18. the loss of FKBP12.6 has no significant effect on the conduction and activation of RyR2 or the propensity for spontaneous Ca(2+) release and stress-induced ventricular arrhythmias PMID: 17921453
19. The findings suggest that FKBP12.6 regulation of RyR2 is unlikely to be the primary defect in inherited arrhythmogenic cardiac disease. PMID: 19226252

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HGNC: 3712

OMIM: 600620

KEGG: hsa:2281

STRING: 9606.ENSP00000370373

UniGene: Hs.709461