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anti-Rat (Rattus) GDNF Antibodies:
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Human Polyclonal GDNF Primary Antibody for ICC, IHC (p) - ABIN3044406
Zhang, Shi, Li, Zhang, Hao: Lipopolysaccharide inhibits the self-renewal of spermatogonial stem cells in vitro via downregulation of GDNF expression in Sertoli cells. in Reproductive toxicology (Elmsford, N.Y.) 2014
Show all 2 Pubmed References
Rat (Rattus) Polyclonal GDNF Primary Antibody for WB - ABIN3042421
Li, Xia, Zhang, Wu: S100B protein, brain-derived neurotrophic factor, and glial cell line-derived neurotrophic factor in human milk. in PLoS ONE 2011
Show all 2 Pubmed References
Human Polyclonal GDNF Primary Antibody for ELISA, IHC - ABIN1585729
Lunn, Sakowski, McGinley, Pacut, Hazel, Johe, Feldman: Autocrine production of IGF-I increases stem cell-mediated neuroprotection. in Stem cells (Dayton, Ohio) 2016
Human Polyclonal GDNF Primary Antibody for IHC, IP - ABIN4313822
Naudin, Smith, Bond, Dun, Scott, Ashman, Weidenhofer, Roselli: Characterization of the early molecular changes in the glomeruli of Cd151-/-mice highlights induction of mindin and MMP-10. in Scientific reports 1970
Human Polyclonal GDNF Primary Antibody for ELISA, WB - ABIN2473775
Lin, Doherty, Lile, Bektesh, Collins: GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons. in Science (New York, N.Y.) 1993
Show all 2 Pubmed References
Human Polyclonal GDNF Primary Antibody for IF (p), IHC (p) - ABIN736536
Zhang, Cai, Song, Dong, Hou, Lv: Normalization of ventral tegmental area structure following acupuncture in a rat model of heroin relapse. in Neural regeneration research 2014
results contradict previous studies suggesting that mammalian GFRalpha1 (show GFRA1 Antibodies) and GDNF cannot bind and activate non-mammalian RET (show RET Antibodies) and vice versa
the dynamics of glial cell line-derived neurotrophic factor (gdnf) and nitric oxide synthases (nos) mRNA expression in various regions of zebrafish brain
GDNF family ligands including tyrosine kinase receptor (show KDR Antibodies) RET (show RET Antibodies) are investigated within the adult zebrafish brain.
GDNF is a major determinant of directed neuritic growth , and GDNF acts by promoting local neurite outgrowth.
These results demonstrated the expression of the GDNF receptorial complex in adult zebrafish cerebellum and suggest an autocrine mode of action of GDNF in Purkinje cells.
These results showed that the expression of GDNF is not probably restricted during development but it might be involved in the physiology of adult zebrafish retina.
The expression of glial cell line-derived neurotrophic factor (GDNF) was not restricted to developmental periods but it seems that this factor might be involved in adult zebrafish brain physiology, as observed in mammals.
Analysis of striatal brain samples confirms increased GDNF expression in lentiviral vector-GDNF treated aged animals that correlates with functional improvements and preserved dopaminergic markers, dependent upon GDNF levels.
Data show that NEDL2 regulates GDNF/Ret/Akt pathway depends on its Nedd8 ligase activity rather than ubiquitin ligase activity.
Six2 (show SIX2 Antibodies) mediates the protective effects of GDNF on damaged DA neurons by regulating Smurf1 (show SMURF1 Antibodies) expression.
Ret (show RET Antibodies) is essential to mediate GDNF's neuroprotective and neuroregenerative effect in a Parkinson disease mouse model.
identified IFNg (show IFNG Antibodies), Neurturin (Nrtn (show NRTN Antibodies)), and glial-derived neurotrophic factor (GDNF) as ligands with unexpected roles in promoting neurogenic differentiation (show NEUROD1 Antibodies) of Neural Precursor Cells in vivo.
Using an organ culture system for prostate development and Ret mutant mice, we demonstrate that RET-mediated GDNF signaling in UGS increases proliferation of mesenchyme cells and suppresses androgen-induced proliferation and differentiation of prostate epithelial cells, inhibiting prostate development.
The GDNF-GFRalpha1 (show GFRA1 Antibodies) complex is essential for proper hippocampal circuit development.
In SOD1 (show SOD1 Antibodies)(G93A) spinal cords, we verified a strict correlation in the expression of the TNFalpha (show TNF Antibodies), TNFR1 (show TNFRSF1A Antibodies) and GDNF triad at different stages of disease progression. Yet, ablation of TNFR1 (show TNFRSF1A Antibodies) completely abolished GDNF rises in both SOD1 (show SOD1 Antibodies)(G93A) astrocytes and spinal cords, a condition that accelerated motor neuron degeneration (show CLN8 Antibodies) and disease progression
GDNF signals were able to induce the stratified aggregate formation of GFRalpha1 (show GFRA1 Antibodies)-positive undifferentiated spermatogonia
Our results show the existence of two subpopulations of peptidergic nociceptors characterized by the presence of CGRP (show CALCA Antibodies), one expressing BDNF (show BDNF Antibodies) (plus SP), the other expressing GDNF (plus SST (show SST Antibodies)), suggesting a different role for these two neurotrophic factors in the discrimination of specific painful stimuli modalities.
The data of this study suggested that short-term exposure to hyperoxic conditions can affect the regulation and expression of BDNF (show BDNF Antibodies) potentially leading to alterations in neural development.
Spatial expression analysis by whole-mount in situ hybridization showed that the GDNF mRNA was predominantly detected in somites, pronephros, pharyngeal arches, epibranchial placodes, digestive tract and some of the lateral line structure.
These findings provide preliminary evidence that silencer II hypermethylation in the gdnf promoter II may underlie high gene transcription in high-grade glioma cells.
there is a decrease in epidermal GDNF and GFRalpha-1 protein expression in normal human skin with ageing
In functional dyspepsia patients, duodenal expression of GDNF protein was significantly increased compared with controls. GDNF was localized in enteric glial cells, eosinophils, and epithelial cells.
Suppression of miR-383 may increase the therapeutic potential of human bone-marrow-derived MSCs in treating spinal cord injury via augmentation of GDNF protein levels.
Our results suggest that GDNF rs3096140 might be involved in the genetic background of smoking, independent of anxiety characteristics.
No correlations between the levels of serum neurotrophins and the severity of ADHD were observed. These results suggest that elevated serum GDNF and NTF3 (show NTF3 Antibodies) levels may be related to ADHD in children.
BDNF (show BDNF Antibodies) and GDNF interact with the 5-HT (show DDC Antibodies)-system of the brain through feedback mechanisms engaged in autoregulation
the synergistic effect of Gas1 (show GAS1 Antibodies) inhibition and GDNF against glutamate (show GRIN1 Antibodies)-induced cell injury in human SH-SY5Y neuroblastoma (show ARHGEF16 Antibodies) cells, is reported.
Study shows no correlation between GDNF rs884344 and rs3812047 polymorphisms and subjects with tinnitus.
This gene encodes a highly conserved neurotrophic factor. The recombinant form of this protein was shown to promote the survival and differentiation of dopaminergic neurons in culture, and was able to prevent apoptosis of motor neurons induced by axotomy. The encoded protein is processed to a mature secreted form that exists as a homodimer. The mature form of the protein is a ligand for the product of the RET (rearranged during transfection) protooncogene. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene may be associated with Hirschsprung disease.
, Glial cell line derived neutrophic factor
, astrocyte-derived trophic factor
, glial cell line derived neurotrophic factor
, glial cell line-derived neurotrophic factor
, glial cell line-derived neurotrophic factor long form
, glial cell derived neurotrophic factor
, glial cell-line derived neurotrophic factor
, neurotrophic factor
, glial cell line-derived neurotrophic factor a
, glia-derived neurotrophic growth factor