IFNAR1 (NM_000629) Human Over-expression Lysate

SKU
LY400212
Transient overexpression lysate of interferon (alpha, beta and omega) receptor 1 (IFNAR1) (as WB positive control)
  $436.00
2 Weeks*
Bulk/Customize
Specifications
Specifications
Product Data
Species Human
Expression Host HEK293T
Expression cDNA Clone or AA Sequence TrueORF Clone RC205141
Tag C-Myc/DDK
Detection Antibodies Clone OTI4C5, Anti-DDK (FLAG) monoclonal antibody (TA50011-100)
ACCN NM_000629, NP_000620
Synonyms AVP; IFN-alpha-REC; IFNAR; IFNBR; IFRC
Predicted MW 63.5 kDa
Components 1 vial of 100 µg total protein derived from gene specific transient over-expression cell lysate in RIPA buffer
1 vial of 100 µg whole HEK293T cell lysate in RIPA buffer
Storage The lysate is shipped with dry ice. Upon receiving, store the sample at -80°C. Also after dilution, the protein sample should be aliquoted and stored at -80°C for long term storage. Avoid repeated freeze-thaw cycles. Lysate samples can be diluted with 1x SDS-PAGE running buffer (with reducing agent). Lysate samples are stable for 12 months from the date of receipt when stored at -80°C. Lysate samples are stable for 12 months from the date of receipt when stored at -80°C.
Shipping Dry Ice
Preparation HEK293T cells in 10-cm dishes were transiently transfected with MegaTran Transfection Reagent (TT200002) and 5ug TrueORF cDNA plasmid. Transfected cells were cultured for 48hrs before collection. The cells were lysed in modified RIPA buffer (25mM Tris-HCl pH7.6, 150mM NaCl, 1% NP-40, 1mM EDTA, 1xProteinase inhibitor cocktail mix (Sigma), 1mM PMSF and 1mM Na3VO4), and then centrifuged to clarify the lysate. Protein concentration was measured by BCA kit (Thermo Scientific Inc.).
Reference Data
RefSeq NP_000620
Locus ID 3454
Cytogenetics 21q22.11
Protein Families WB
Protein Pathways Cytokine-cytokine receptor interaction, Jak-STAT signaling pathway, Natural killer cell mediated cytotoxicity, Toll-like receptor signaling pathway
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Other "IFNAR1" proteins (3)
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file-alt Citations

Type-1 interferons contribute to oxygen glucose deprivation induced neuro-inflammation in BE(2)M17 human neuroblastoma cells
Minter, Zhang, Ates et al
J Neuroinflammation (2014) 11 (1), 43 DOI: 10.1186/1742-2094-11-43
Cited by 17
AI Summary: OriGene’s shRNA plasmid constructs targeting IFNAR1 and a non-effective scrambled shRNA control were used to generate knockdown and control BE(2)M17 cell lines, enabling the study to demonstrate the role of type-1 interferon signaling in neuro-inflammation following oxygen glucose deprivation.
Snippet: IFNAR1(IFNAR1KD)ornegativecontrol(NC)knock- downM17cellsweregeneratedusingcommercially availableshRNAplasmidconstructs(Origene).Briefly, M17cellsweretransfectedusingFugene<00AE>HD(Promega) withshRNAplasmidscontaininganIFNAR1specific shRNAcassetteornon-effective29-merscrambledshRNA cassettewithaGFPtag.Clonalcelllinesweregenerated
Showing 1-1 of 1 papers.
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