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Human Polyclonal FTH1 Primary Antibody für WB - ABIN515829
Kim, Moore, Fussenegger: Genetically programmed superparamagnetic behavior of mammalian cells. in Journal of biotechnology 2012
Human Polyclonal FTH1 Primary Antibody für IF (p), IHC (p) - ABIN759641
Zhang, Zhao, Chang, Zhang, Chu, Zhang, Liu, Guo, Wang, Gao, Zhang, Chu: Calcium channel blockers ameliorate iron overload-associated hepatic fibrosis by altering iron transport and stellate cell apoptosis. in Toxicology and applied pharmacology 2016
Cow (Bovine) Polyclonal FTH1 Primary Antibody für IHC, WB - ABIN2785803
Sammarco, Ditch, Banerjee, Grabczyk: Ferritin L and H subunits are differentially regulated on a post-transcriptional level. in The Journal of biological chemistry 2008
Show all 2 Pubmed References
CD16 (zeige CD16 Antikörper) expression and morphological maturity of neutrophils are associated with higher iron ferritin (zeige FTL Antikörper) levels in major beta-thalassemia.
Study demonstrate that the amounts of ferritin heavy subunit are inversely correlated, in K562 cells, to H19 (zeige NCKAP1 Antikörper)/miR (zeige MLXIP Antikörper)-675 levels, and that this phenomenon may be largely attributed to the increase in ROS (zeige ROS1 Antikörper) production induced by the FHC silencing.
Findings indicate that induction of EMT (zeige ITK Antikörper), increased migration and survival depend, in MCF-7 and H460 cells, on the release of FHC control on two pathways, namely the iron/ROS (zeige ROS1 Antikörper) metabolism and CXCR4 (zeige CXCR4 Antikörper)/CXCL12 (zeige CXCL12 Antikörper) axis.
ferritin heavy chain has a role in ovarian cancer stem cell expansion and epithelial to mesenchymal transition
Report in vivo magnetic resonance imaging of xenografted neuroblastoma (zeige ARHGEF16 Antikörper) tumors using FTH1 reporter gene expression controlled by a tet-on switch.
The H-ferritin could bind up to 24 NCOA4 (zeige NCOA4 Antikörper)(383-522) fragments forming highly stable and insoluble complexes. The binding was partially inhibited only by Fe(II) among the various divalent metal ions analyzed. The iron-dependent, highly-specific formation of the remarkably stable H-ferritin-NCOA4 (zeige NCOA4 Antikörper) complex shown in this work may be important for the characterization of the mechanism of ferritinophagy.
Recombinant human H-chain ferritin (zeige FTL Antikörper) nanocages were characterized by transmission electron microscopy and dynamic light scattering. These results indicate that H-chain ferritin (zeige FTL Antikörper) is able to self-assemble into nanocages with a narrow size distribution.
Among myelodysplastic syndromes patients only, CD163 (zeige CD163 Antikörper) + macrophage density and HO1 (zeige HMOX1 Antikörper) and H-ferritin expression by CD163 (zeige CD163 Antikörper) + macrophages increased in tandem with marrow iron. High HO1 (zeige HMOX1 Antikörper) was significantly associated with shorter overall survival.
Low levels of FTH-positive tumor cells and microglia/macrophages were associated with poor survival in anaplastic astrocytomas, while high amounts of FTL (zeige FTL Antikörper)-positive microglia/macrophages had a negative prognostic value
fumarate increases ferritin (zeige FTL Antikörper) gene transcription by activating the NRF2 (zeige GABPA Antikörper) (nuclear factor [erythroid-derived 2]-like 2) transcription factor.
Ferritin H subunit gene is specifically expressed in melanophore precursor-derived white pigment cells
ferritin heavy chain up-regulation may be mediated by activation of NF-kappaB (zeige NFKB1 Antikörper) and that in turn this may be related to the resistance of bovine papillomavirus type-2 (BPV-2) infected urothelial cells to apoptosis.
FtMt (zeige FTMT Antikörper) overexpressing mice have no significant defects and the overexpression of FtMt (zeige FTMT Antikörper) does not affect the regulation of iron metabolism significantly in transgenic mice.
Ferritin (zeige FTL Antikörper) is considered the major iron storage protein which maintains a large iron core in its cavity and has ferroxidase (zeige CP Antikörper) activity. (Review)
the absence of Mitochondrial ferritin (zeige FTMT Antikörper), which is highly expressed in the heart, increases the sensitivity of mitochondria to cardiac injury via oxidative stress.
As previously reported, homozygous loss of the Fth allele on a wild-type Ftl (zeige FTL Antikörper) background was embryonic lethal. expression of the H subunit can rescue the loss of the L subunit and that H ferritin homopolymers have the capacity to sequester iron in vivo
provide a new mechanism for selective autophagy of ferritin (zeige FTL Antikörper) and reveal a previously unappreciated role for autophagy and NCOA4 (zeige NCOA4 Antikörper) in the control of iron homeostasis in vivo
Our data show that ferritin H (zeige FTMT Antikörper) is required for B and T cell survival by actively reducing the labile iron pool.
Ferritin H (zeige FTMT Antikörper) deficiency in most cells of the forebrain including cells of the choroid plexus caused accumulation of cerebrospinal fluid in the lateral ventricles and the subarachnoid space
Mycobacterium avium infection induces H-ferritin expression in mouse primary macrophages by activating Toll-like receptor 2.
3-Hydroxybutyrate dehydrogenase (zeige BDH1 Antikörper)-2 and ferritin-H (zeige FTMT Antikörper) synergistically regulate intracellular iron.
Fth plays a critical protective role during acute kidney injury.
The X-ray crystal structure of the apoferritin-SDS (zeige SDS Antikörper) complex was determined at a resolution of 1.9 A and revealed that the SDS (zeige SDS Antikörper) binds in an internal cavity that has previously been shown to recognize various general anesthetics. [apoferritin]
This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined.
, cell proliferation-inducing gene 15 protein
, ferritin H subunit
, ferritin heavy chain
, placenta immunoregulatory factor
, proliferation-inducing protein 15
, ferritin H chain
, ferritin H subunit A
, ferritin heavy chain 2
, ferritin heavy chain A
, ferritin H subunit B
, ferritin heavy chain 1
, ferritin heavy chain B
, ferritin, heavy polypeptide 1 b
, ferritin heavy polypeptide 1
, ferritin heavy-chain
, Ferritin subunit H
, ferritin, heavy polypeptide 1
, Ferritin H subunit