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Human Polyclonal FUCA1 Primary Antibody für IF (p), IHC (p) - ABIN682003
Gustafson, Shepherd, Miller, Jayachandran: Age- and sex-specific differences in blood-borne microvesicles from apparently healthy humans. in Biology of sex differences 2015
Human Monoclonal FUCA1 Primary Antibody für WB - ABIN395006
Nandakumar, Hsu, Lin, Lo, Lo, Lin: Detection of Human ?-L-Fucosidases by a Quinone Methide-Generating Probe: Enhanced Activities in Response to Helicobacter pylori Infection. in Chembiochem : a European journal of chemical biology 2015
Homozygous frameshift mutation in the FUCA1 gene causes both severe and mild fucosidosis.
alterations in plasma levels of FUCA-1 were significantly associated with chronic inflammatory and autoimmune disorders, both in children and adults
the down-regulation of FUCA-1 correlates with increased aggressiveness of the cancer type. This is the first report indicating that the down-regulation of FUCA-1 is related to the increased aggressiveness of thyroid cancer.
the possibility that the higher fucose levels on cell surface glycans of aggressive anaplastic thyroid cancer samples (ATCs), compared to those of less aggressive papillary thyroid cancer samples(PTC), may be at least in part responsible for the more aggressive and metastatic phenotype of ATCs compared to PTCs, as the expression levels of FUCA1 and FUT8 were inversely related in these two types of cancers.
RNAi-mediated knockdown of endogenous FUCA1 significantly attenuates p53-dependent, chemotherapy-induced apoptotic death.
whole exome sequencing and array-based comparative genomic hybridization analysis revealed that the patient was compound heterozygous for a single base-pair deletion inherited from his father, and a 3281-base-pair deletion covering exon 3 inherited from his mother. Neither mutation has been reported before so the FUCA1 mutational spectrum is herein expanded.
results show that protein defucosylation mediated by FUCA1 is involved in tumor suppression
FUCA1 downregulation confers inferior survival for triple-negative breast cancer patients by modulating the glycosylation status of the tumor cell surface
We observed significant lower values of GAL, alpha-fucosidase and tendency to decrease of MAN and GLU concentration in nasal polyps
Serum alpha-L-fucosidase levels were significantly elevated in hepatocellular carcinoma.
IL-13, IL-4 and IL-5 have no effect on the expression of FUCA1 and FUCA2, but its expression is upregulated by IFN-gamma, a Th1 cytokine.
Preoperative serum AFU is a prognostic predictor of hepatocellular carcinoma.
Diminished FUCA1 mRNA levels in tumors, indicate that expression of tissue alpha-L-fucosidase could be regulated at transcriptional level in colorectal cancer.
In the serum of patients with Lyme disease, GAL activity significantly increased (p = 0.029), and the activity of FUC had a tendency to increase (p = 0.153), compared to the control group.
Data show that the correlation between the fluorescence activity of the enzyme AFU by the developed procedures and the standard method was positive and highly significant in patients and controls.
The purified alpha-L-fucosidase from primary hepatocarcinoma (PHC) is different in its properties from alpha-L-fucosidase in human other organs. The polyclonal antibody prepared in this experiment can be applied to the diagnosis of PHC.
The fucosidase has a role in the intimate species signature interactions between sperm and oocyte.
following HIV infection, there is an increased rate of catabolism of glycoconjugates in saliva resulting from changes in the proportions of the activity of isoenzymes A and B of N-acetyl-beta-hexosaminidase, beta-galactosidase and alpha-fucosidase
The results showed that FUC1 is an alpha-1,3-fucosidase acting on plant complex-type N-glycans and elucidated the degradation pathway of plant complex-type N-glycans.
The protein encoded by this gene is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. Mutations in this gene are associated with fucosidosis (FUCA1D), which is an autosomal recessive lysosomal storage disease. A pseudogene of this locus is present on chr 2.
, alpha-L-fucosidase I
, alpha-L-fucoside fucohydrolase 1
, tissue alpha-L-fucosidase
, fucosidase, alpha-L- 1, tissue
, fucosidase, alpha-L-1, tissue
, Fucosidase alpha-L-1 tissue
, Fucosidase, alpha-L-1, tissue
, tissue alpha-L-fucosidase-like