ULK2 rabbit pAb
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ULK2 rabbit pAb
Background :
Unc-51 like autophagy activating kinase 2 (ULK2) Homo sapiens This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]Description :
Unc-51 like autophagy activating kinase 2 (ULK2) Homo sapiens This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008],UniProt :
Q8IYT8Swiss Prot :
Q8IYT8Reactivity :
Human; Mouse; RatImmunogen :
Synthetic peptide from human protein at AA range: 930-1000Clonality :
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 :
Cytoplasmic vesicle membrane ; Peripheral membrane protein . Localizes to pre-autophagosomal membrane.Other Product Names :
ULK2 KIAA0623Gene ID (Human) :
9706

