AMBRA1 rabbit pAb
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AMBRA1 rabbit pAb
Background:
Function:Regulates autophagy and development of the nervous system. Involved in autophagy in controlling protein turnover during neuronal development, and in regulating normal cell survival and proliferation., similarity:Contains 3 WD repeats., subunit:Interacts with BECN1. Probably forms a complex with BECN1 and PIK3C3.Description:
Function: Regulates autophagy and development of the nervous system. Involved in autophagy in controlling protein turnover during neuronal development, and in regulating normal cell survival and proliferation. similarity: Contains 3 WD repeats. subunit: Interacts with BECN1. Probably forms a complex with BECN1 and PIK3C3.UniProt:
Q9C0C7Swiss Prot:
Q9C0C7Reactivity:
Human; MouseImmunogen:
Synthetic Peptide of AMBRA1Clonality:
PolyclonalSource:
RabbitApplications:
WB; ELISAConcentration:
1 mg/mlDilution:
WB 1:500-2000, ELISA 1:10000-20000Molecular Weight:
140kDStorage Conditions:
-20°C/1 yearObserved Molecular Weight:
140kDFragment:
IgGSubcellular Location:
Endoplasmic reticulum . Cytoplasm, cytoskeleton . Cytoplasmic vesicle, autophagosome . Mitochondrion . Cytoplasm, cytosol . Nucleus . Cell junction, focal adhesion . Localizes to the cytoskeleton in absence of autophagy induction (PubMed:20921139) . Upon autophagy induction, AMBRA1 relocalizes to the endoplasmic reticulum to enable autophagosome nucleation (PubMed:20921139) . Partially localizes at mitochondria in normal conditions (PubMed:21358617) . Localizes also to discrete punctae along the ciliary axoneme (By similarity) . .Other Product Names:
Autophagy/beclin-1 regulator 1Gene ID (Human):
55626
