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anti-Human Aspartate beta Hydroxylase Antikörper:
anti-Mouse (Murine) Aspartate beta Hydroxylase Antikörper:
anti-Rat (Rattus) Aspartate beta Hydroxylase Antikörper:
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Higher levels of HAAH/humbug mRNA were found in the hepatocellular carcinoma tissues relative to the adjacent cancerfree tissue.
this study provides evidence that ASPH is mutated in a distinct form of syndromic ectopia lentis.
Data show that junctate (ASPH) is an interacting partner of Orai1 (zeige ORAI1 Antikörper)-STIM1 (zeige STIM1 Antikörper) complex.
Ca(2 (zeige CA2 Antikörper)+) and JNT-dependent disassembly of the CSQ2 polymer
Aspartyl-asparaginyl-beta-hydroxylase is an important, positive regulator of trophoblastic cell motility, and it's inhibition in vivo leads to impaired implantation and fetal growth, and alters Notch (zeige NOTCH1 Antikörper)-signaling mechanisms.
Low expression of AAH in the endochylema and nucleus of trephocyte may play a role in patients with missed abortion.
role of gene in neuroblastoma (zeige ARHGEF16 Antikörper) cell motility
AAH over-expression may contribute to the infiltrative growth pattern of cholangiocarcinoma cells by promoting motility.
junctate has a role in calcium homeostasis in eukaryotic cells
This review summarizes recent progress in elucidating the molecular mechanisms of hypoxia-inducible factor (HIF)-1 (zeige HIF1A Antikörper) activation, focusing on the role of oxygen-dependent prolyl hydroxylase in hypoxia signal transduction.
Results predict that junctin ablation, or mutations that alter its structural attributes, may mimic the etiology of catecholaminergic polymorphic ventricular tachycardia by causing enhanced diastolic Ca2 (zeige CA2 Antikörper)+ leak in the presence of beta-adrenergic activation.
in skeletal muscle the disruption of Tdn (zeige TRDN Antikörper)/CASQ (zeige CASQ1 Antikörper) link has a more profound effect on jSR architecture and myoplasmic Ca(2 (zeige CA2 Antikörper)+) regulation than Jct/CASQ (zeige CASQ1 Antikörper) association.
junctate may play an important role in the regulation of sarcoplasmic reticulum Ca(2 (zeige CA2 Antikörper)+) cycling through the interaction with SERCA2a (zeige ATP2A2 Antikörper) in the murine heart.
Cardiac remodeling and atrial fibrillation in transgenic mice overexpressing junctin
the N-terminus of junctate interacts with the C-terminus of TRPC2 (zeige TRPC2 Antikörper)
To gain more insight into the underlying mechanisms of impaired contractile relaxation in transgenic mice with cardiac-specific overexpression of junctin (TG), we studied cellular Ca(2 (zeige CA2 Antikörper)+) handling in these mice.
Junctin is an essential regulator of sarcoplasmic reticulum Ca release and contractility in normal hearts. Ablation of junctin is associated with aberrant Ca homeostasis, which leads to fatal arrhythmias
Data suggest that junctate over-expression is associated with an increase in the sarcoplasmic reticulum Ca2 (zeige CA2 Antikörper)+ storage capacity and releasable Ca2 (zeige CA2 Antikörper)+ content and support a physiological role for junctate in intracellular Ca2 (zeige CA2 Antikörper)+ homeostasis.
review of recent findings concerning the expressional regulations and the proposed functions of junctin and junctate
This gene is thought to play an important role in calcium homeostasis. The gene is expressed from two promoters and undergoes extensive alternative splicing. The encoded set of proteins share varying amounts of overlap near their N-termini but have substantial variations in their C-terminal domains resulting in distinct functional properties. The longest isoforms (a and f) include a C-terminal Aspartyl/Asparaginyl beta-hydroxylase domain that hydroxylates aspartic acid or asparagine residues in the epidermal growth factor (EGF)-like domains of some proteins, including protein C, coagulation factors VII, IX, and X, and the complement factors C1R and C1S. Other isoforms differ primarily in the C-terminal sequence and lack the hydroxylase domain, and some have been localized to the endoplasmic and sarcoplasmic reticulum. Some of these isoforms are found in complexes with calsequestrin, triadin, and the ryanodine receptor, and have been shown to regulate calcium release from the sarcoplasmic reticulum. Some isoforms have been implicated in metastasis.
, similar to Aspartyl/asparaginyl beta-hydroxylase (Aspartate beta-hydroxylase) (ASP beta-hydroxylase) (Peptide-aspartate beta-dioxygenase)
, A beta H-J-J
, ASP beta-hydroxylase
, aspartyl/asparaginyl beta-hydroxylase
, cardiac junctin
, peptide-aspartate beta-dioxygenase
, junctional sarcoplasmic reticulum protein
, aspartyl beta-hydroxylase
, calsequestrin-binding protein