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Product Info Summary
|Description:||Transient overexpression lysate of RAD23 homolog A (S. cerevisiae) (RAD23A)|
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hHR23A (RAD23A) (NM_005053) Human Over-expression Lysate
Transient overexpression lysate of RAD23 homolog A (S. cerevisiae) (RAD23A)
Storage & Handling
Cite This Product
hHR23A (RAD23A) (NM_005053) Human Over-expression Lysate (Boster Biological Technology, Pleasanton CA, USA, Catalog # LS005886)
Clone OTI4C5, Anti-DDK (FLAG) monoclonal antibody (M30971)
HEK293T cells in 10-cm dishes were transiently transfected with Transfection Reagent and 5ug ORF 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, 1mM PMSF and 1mM Na3VO4), and then centrifuged to clarify the lysate. Protein concentration was measured by BCA kit. Cell lysates were aliquoted and stored at -20°C before shipping.
Validation Images & Assay Conditions
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hHR23A (RAD23A) Human Over-expression Lysates NM_005053.
Western blot validation of overexpression lysate (LS005886) using anti-DDK antibody. Left: Cell lysates from un-transfected HEK293T cells; Right: Cell lysates from HEK293T cells transfected with RAD23A (Myc-DDK-tagged) Human Tagged ORF Clone using transfection reagent.
Gene/Protein Information for RAD23A (Source: Uniprot.org, NCBI)
UV excision repair protein RAD23 homolog A
hHR23; Rad23 RAD23A HHR23A, HR23A RAD23 homolog A, nucleotide excision repair protein UV excision repair protein RAD23 homolog A|RAD23, yeast homolog, A*If product is indicated to react with multiple species, protein information is based on the gene entry specified above in "Species".
For more info on RAD23A, check out the RAD23A Infographic
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In this infographic, you will see the following information for RAD23A: database IDs, superfamily, protein function, synonyms, molecular weight, chromosomal locations, tissues of expression, subcellular locations, post-translational modifications, and related diseases, research areas & pathways. If you want to see more information included, or would like to contribute to it and be acknowledged, please contact us [email protected]
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