GFRαL, or GDNF Family Receptor Alpha-Like, is a relatively newly identified member of the GDNF receptor family, which are receptors known to play pivotal roles in the survival and maintenance of various neuron populations. Like its counterparts, GFRαL likely functions as a receptor for members of the GDNF family of ligands, which are essential for neural cell survival, development, and function. Although the specific ligands and exact physiological roles of GFRαL are not fully defined, it is suggested that GFRαL might be involved in similar signaling pathways that promote neuronal survival and could be crucial in specific contexts of brain development or in response to neuronal injury. Given its potential role in neural health, GFRαL could be critical in understanding neurodegenerative diseases and could serve as a target for therapeutic interventions aimed at neuroprotection and regeneration.
The inhibition of GFRαL can lead to disruptions in the signaling pathways that are vital for neuron survival and functionality. One possible mechanism of inhibition could be through the binding of antagonistic molecules that competitively block the interaction between GFRαL and its natural ligands. These antagonists could mimic the structure of the natural ligands but fail to induce the receptor's typical response, effectively silencing the receptor's activity. Another significant method of inhibition could involve alterations in the expression levels of GFRαL, whether through transcriptional repression or through epigenetic mechanisms that modify the accessibility of the GFRαL gene in the genome. Such changes could result in lowered synthesis of the receptor, diminishing its presence on the cell surface and thereby its ability to partake in critical signaling processes. Additionally, post-translational modifications such as phosphorylation, ubiquitination, or cleavage could affect the stability or cellular localization of GFRαL, further impairing its functionality.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $26.00 $92.00 $120.00 $310.00 $500.00 $908.00 $1821.00 | 46 | |
A tyrosine kinase inhibitor; might influence proteins involved in tyrosine kinase pathways. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
PI3K inhibitor; can modulate proteins associated with PI3K pathway. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
An ERK inhibitor; proteins related to ERK signaling can be modulated. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
ROCK inhibitor; might affect proteins in pathways involving Rho-associated kinase. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
Src family kinase inhibitor; can influence proteins linked to Src kinase signaling. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
A broad-spectrum kinase inhibitor; can affect multiple kinase-related pathways. | ||||||
Calphostin C | 121263-19-2 | sc-3545 sc-3545A | 100 µg 1 mg | $336.00 $1642.00 | 20 | |
PKC inhibitor; if GFRαL is associated with PKC signaling, this can modulate its activity. | ||||||
Tyrphostin B42 | 133550-30-8 | sc-3556 | 5 mg | $26.00 | 4 | |
JAK-STAT pathway inhibitor; can modulate proteins associated with JAK-STAT signaling. | ||||||
PD173074 | 219580-11-7 | sc-202610 sc-202610A sc-202610B | 1 mg 5 mg 50 mg | $46.00 $140.00 $680.00 | 16 | |
FGFR inhibitor; if GFRαL is involved in FGFR signaling, this can modulate its function. | ||||||
SU 5402 | 215543-92-3 | sc-204308 sc-204308A | 1 mg 5 mg | $62.00 $96.00 | 36 | |
FGF receptor tyrosine kinase inhibitor; can influence FGF-mediated signaling. | ||||||