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
