NUP98 Antibody Summary
Immunogen |
Recombinant protein encompassing a sequence within the C-terminus region of human NUP98. The exact sequence is proprietary.
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Localization |
Nucleus; nuclear pore complex; Nucleus membrane; Peripheral membrane protein; Nucleoplasmic side
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Marker |
Nuclear Pore Complex Marker
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Predicted Species |
Mouse (98%), Rat (98%). Backed by our 100% Guarantee.
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Isotype |
IgG
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Clonality |
Polyclonal
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Host |
Rabbit
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Gene |
NUP98
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Purity |
Immunogen affinity purified
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Applications/Dilutions
Dilutions |
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Application Notes |
The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
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Theoretical MW |
198 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
Packaging, Storage & Formulations
Storage |
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
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Buffer |
0.1M Tris (pH 7.0), 0.1M Glycine and 20% Glycerol
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Preservative |
0.01% Thimerosal
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Concentration |
1 mg/ml
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Purity |
Immunogen affinity purified
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Alternate Names for NUP98 Antibody
- ADAR2
- ADIR2
- GLFG-repeat containing nucleoporin
- nuclear pore complex protein Nup98-Nup96
- nucleoporin 98kD
- nucleoporin 98kDa
- NUP196
- NUP96
- Nup98-Nup96
Background
Signal-mediated nuclear import and export proceed through the nuclear pore complex (NPC), which is comprised of approximately 50 unique proteins collectively known as nucleoporins. The 98 kD nucleoporin is generated through a biogenesis pathway that involves synthesis and proteolytic cleavage of a 186 kD precursor protein. This cleavage results in the 98 kD nucleoporin as well as a 96 kD nucleoporin, both of which are localized to the nucleoplasmic side of the NPC. Rat studies show that the 98 kD nucleoporin functions as one of several docking site nucleoporins of transport substrates. The human gene has been shown to fuse to several genes following chromsome translocatons in acute myelogenous leukemia (AML) and T-cell acute lymphocytic leukemia (T-ALL). This gene is one of several genes located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described. [provided by RefSeq]