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NF-κB p65 subunit (human) (12-317), (recombinant) (GST-tag)

 
BML-UW9990-0050 50 µg 200.00 USD
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Product Specification

MW:~60kDa
 
Source:Produced in E. coli BL21 (λDE3). Recombinant human NF-κB p65 subunit (12-317) is fused to a GST-tag.
 
UniProt ID:Q04206
 
Formulation:Liquid. In 50mM HEPES, pH 7.5, containing 50mM sodium chloride and 1mM DTT.
 
Purity:≥85% (SDS-PAGE)
 
Purity Detail:Purified by multi-step chromatography.
 
Application Notes:For NF-κB pathway studies.
 
Shipping:Shipped on Dry Ice
 
Long Term Storage:-80°C
 
Handling:Avoid freeze/thaw cycles. After opening, prepare aliquots and store at -80°C.
 
Scientific Background:The eukaryotic nuclear factor κB (NF-κB) plays an important role in inflammation, autoimmune response, cell proliferation, and apoptosis by regulating the expression of genes involved in these processes. Misregulation of the NF-κB signal transduction pathway is observed in a variety of human cancers, especially those of lymphoid cell origin. The prototypical inducible NF-κB is a heterodimeric complex consisting of p50 and p65, which normally exists in the cytoplasm of the cell as an inactive form due to association with its major inhibitory protein, IκBα. IκBα prevents the transport of NF-κB into the nucleus by masking its nuclear localization signal. Activation of NF-κB by extracellular inducers depends on the phosphorylation and subsequent degradation of IκBα by the ubiquitin-proteasome pathway.
p65 subunit
The NF-κB p65 subunit is usually thought of as conferring the activation function of the NF-κB complex, though its capacity to associate with κB DNA in the absence of p50 and its potential utility as an independent transcription factor have also been demonstrated.
 
BML-UW9990 SDS PAGE
SDS-PAGE Analysis: Lane 1: MWM; Lane 2: 0.5 µg; Lane 3: 1.0 µg; Lane 4: 2.0 µg; Lane 5: 5.0 µg of purified NF-κB p65 Subunit (12-317) (human) (recombinant) (GST-tag) Protein Prod. No. BML-UW9990.
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BML-UW9990 SDS PAGE

Product Literature References

N-acetyl-l-cysteine sensitizes pancreatic cancers to gemcitabine by targeting the NFκB pathway: S. Qanungo, et al.; Biomed. Pharmacother. 68, 855 (2014), Abstract; Full Text

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