Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
FTL encodes the light subunit of the ferritin protein. Additionally we are shipping FTL Kits (42) and FTL Proteins (24) and many more products for this protein.
Showing 10 out of 230 products:
Human Polyclonal FTL Primary Antibody for ELISA, EIA - ABIN451634
Gu, Xu, Han, Dai, Hao, Wang, Gu, Xu, Cao: The internalization pathway, metabolic fate and biological effect of superparamagnetic iron oxide nanoparticles in the macrophage-like RAW264.7 cell. in Science China. Life sciences 2011
Show all 3 references for ABIN451634
Cow (Bovine) Polyclonal FTL Primary Antibody for EIA, IHC (p) - ABIN375068
Hulliger: Markov-type evolution of materials into a polar state. in Chemistry (Weinheim an der Bergstrasse, Germany) 2002
Show all 2 references for ABIN375068
Cow (Bovine) Polyclonal FTL Primary Antibody for WB - ABIN2785638
Ohta, Nagasaka, Shindo, Toma, Nagasaka, Ohta, Shiozawa: Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene. in Neurology 2008
Human Polyclonal FTL Primary Antibody for EIA, IHC - ABIN334402
Sammarco, Ditch, Banerjee, Grabczyk: Ferritin L and H subunits are differentially regulated on a post-transcriptional level. in The Journal of biological chemistry 2008
Analysis of Ftl-/- mice revealed systemic and brain iron dyshomeostasis, without any noticeable signs of neurodegeneration.
Noncoding G-to-T transversion (c.-168G>T) located in the iron response element (IRE) of the gene coding for ferritin light chain (FTL) cosegregated with cataract in the family.
Ferritin H subunit (show FTH1 Antibodies) gene is specifically expressed in melanophore precursor-derived white pigment cells
Hepatitis E virus ORF1 (show NCKIPSD Antibodies) encoded macro domain protein interacts with light chain subunit of human ferritin and inhibits its secretion.
Ferritin light chain and ferritin heavy chain (show FTH1 Antibodies) are required for the neural differentiation of bone marrow-derived mesenchymal stem cells under extremely low-frequency electromagnetic field.
This study demostrated that FTL mutation progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits show
FTL expression was higher in glioblastoma than in low-grade glioma, and decreased expression of FTL correlated with increased survival in glioblastoma patients.
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy
Ferritin plasma levels increased significantly following stem cell transplantation in graft rejection patients.
Studies indicate that the the best characterized cytosolic ferritins in mammals are encoded by two genes, FTH (show FTH1 Antibodies) and FTL, with four exons and similar structures.
Single nucleotide polymorphisms in HAMP (show HAMP Antibodies), BMP2 (show BMP2 Antibodies), FTL and SLC40A1 (show SLC40A1 Antibodies) genes have phenotype-modifying roles in hereditary hemochromatosis (show HFE Antibodies) type 1.
Genome-wide association study identifies variants in PMS1 (show PMS1 Antibodies) associated with serum ferritin in a Chinese population.
Data suggest that iron-independent effects of ferritin in myeloma should be prospectively investigated in preclinical and clinical studies.
Transmission electron microscopy shows a clear selectivity of alkylated ferritin adsorption onto the PCL (show PKD2L1 Antibodies) phase while wild ferritin predominantly adsorbs onto the PDTD phase.
This gene encodes the light subunit of the ferritin protein. Ferritin is 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 this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes.
ferritin, light polypeptide
, ferritin L subunit 1
, ferritin H subunit A
, ferritin heavy chain 2
, ferritin heavy chain A
, ferritin light-chain
, ferritin L subunit
, ferritin light chain
, ferritin L-chain
, ferritin light polypeptide-like 3
, ferritin light chain 2
, ferritin light chain 1