TPX2; C20orf1; C20orf2; DIL2; HCA519; Targeting protein for Xklp2; Differentially expressed in cancerous and non-cancerous lung cells 2; Hepatocellular carcinoma-associated antigen 519; Protein fls353; Restricted expression proliferation-associated protein
Key Feature
Clonality
Monoclonal
Isotype
IgG1
Clone Number
19AT738.292
Host Species
Mouse
Tested Applications
WB
WB:1:100~500
Species Reactivity
Human
Concentration
1mg/ml
Target Information
Gene Synonyms
C20orf1 C20orf2 DIL2 HCA519
Alternative Names
TPX2 C20orf1 C20orf2 DIL2 HCA519 Targeting protein for Xklp2 Differentially expressed in cancerous and non-cancerous lung cells 2 Hepatocellular carcinoma-associated antigen 519 Protein fls353 Restricted expression proliferation-associated protein
Molecular Weight(MW)
85653 Da
Function
Spindle assembly factor. Required for normal assembly of mitotic spindles. Required for normal assembly of microtubules during apoptosis. Required for chromatin and/or kinetochore dependent microtubule nucleation. Mediates AURKA localization to spindle microtubules. Activates AURKA by promoting its autophosphorylation at 'Thr-288' and protects this residue against dephosphorylation
Tissue Specificity
Expressed in lung carcinoma cell lines but not in normal lung tissues
Cellular Localization
Nucleus. Cytoplasm, cytoskeleton, spindle. Cytoplasm, cytoskeleton, spindle pole. Note=During mitosis it is strictly associated with the spindle pole and with the mitotic spindle, whereas during S and G2, it is diffusely distributed throughout the nucleus. Is released from the nucleus in apoptotic cells and is detected on apoptotic microtubules
Western analysis of extracts from Jurkat cells using P100 antibody.
Application Notes
WB:1:100~500
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer
Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.