抗Mouse (Murine) SLC39A3 抗体:
抗Human SLC39A3 抗体:
抗Rat (Rattus) SLC39A3 抗体:
Human Polyclonal SLC39A3 Primary Antibody for WB - ABIN949250
Kanninen, Grubman, Caragounis, Duncan, Parker, Lidgerwood, Volitakis, Ganio, Crouch, White: Altered biometal homeostasis is associated with CLN6 mRNA loss in mouse neuronal ceroid lipofuscinosis. in Biology open 2013
ZnT3 KO mice showed abnormality in trace fear conditioning is involved in associative fear memory and extinction, but not in innate fear.
Znt-3-deficient mice lacking synaptic Zn also show less hippocampal cell damage following kainic acid injection. Zip transporters may provide selective therapeutic targets to protect these neurons from early Zn-induced neurodegeneration following injury.
The expression of zinc transporter 3 (ZnT3) starts early in development, lasts throughout embryonic life, and is detected in proliferative and differentiating areas of the brain in distinct chelatable vesicular zinc pools.
ZnT3-immunoreactive ependymal cells possess secretory activity directed towards the central canal.
ZIP1, ZIP2 and ZIP3 may play cell-specific roles in zinc homeostasis rather than primary roles in the acquisition of dietary zinc
ZIP1 and ZIP3 zinc uptake transporter activity is controlled by zinc-stimulated endocytosis
Reduced expression of Zip3 ultimately resulted in cell death, indicating that mammary epithelial cells have a unique requirement for Zip3-mediated Zn(2+) import.
Knockout mice lacking Zip3 were generated and characterized.
Mutations in the ZIP1 and ZIP3 zinc transporter genes are silent when dietary intake of zinc is normal, but can dramatically compromise the success of pregnancy when dietary intake of zinc is limiting.
temporal and spatial patterns of expression of the mouse ZIP1, 3, 4, and 5 genes in the developing intestine and the effects of maternal dietary zinc deficiency on these patterns of expression were examined
Slc39a3 apparently plays a critical role in zinc homeostasis when zinc is replete, but they play important, noncompensatory roles when this metal is deficient
Zip3 does not participate in the acquisition of Zn from maternal circulation for secretion into milk but, in contrast, primarily plays a role in the reuptake and cellular retention of Zn in the mammary gland from the previously secreted milk pool.
These results support a concept that downregulation of RREB-1 causes downregulation of ZIP3, which results in decreased zinc in pancreatic premalignant and carcinoma cells
The metallothionein gene had a higher expression in the blood, when compared to zinc transporters ZnT-1, Zip-1, and Zip-3 (p=0.01 in obese patients.
Data show that the combination of concurrent zinc, ZIP3, and RREB-1 changes represent early events in the development of adenocarcinoma.
ZiP2 and Zip3 are down regulated in malignant cells
Gene expression regulation of ZIPs after zinc supplementation.
This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone.
, solute carrier family 39 member 3
, zinc transporter ZIP3
, zrt- and Irt-like protein 3