| HepG2 | 
Caption: IP-Western Blot analysis of HepG2 whole cell lysate using CIP29 specific antibody. Lane 1 is 1% of twenty million whole cell lysate input and lane 2 is 25% of IP enrichment using rabbit normal IgG (lanes under 'IgG'). Lane 3 is 1% of twenty million whole cell lysate input and lane 4 is 10% IP enrichment using rabbit polyclonal anti-CIP29 antibody (lanes under 'CIP29'). Method: immunoprecipitation Status: Released Lab: Yeo Lab | 
Caption: Western blot following shRNA against SARNP in HepG2 whole cell lysate using SARNP specific antibody. Lane 1 is a ladder, lane 2 is HepG2 non-targeting control knockdown, lane 3 and 4 are two different shRNA against SARNP. SARNP protein appears as the green arrow, Tubulin serves as a control and appears in red arrow. Releated Sample: BGHLV18-55 Status: NotSatisfied Lab: Graveley Lab 
Caption: Western blot following CRISPR against SARNP in HepG2 whole cell lysate using SARNP specific antibody. Lane 1 is a ladder, lane 2 is HepG2 non-targeting control knockdown, lane 3 and 4 are two different CRISPR against SARNP. SARNP protein appears as the green arrow, Beta-actin serves as a control and appears in red arrow. Releated Sample: BGHcLV31-27 Status: Released Lab: Graveley Lab |
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| K562 | 
Caption: IP-Western Blot analysis of K562 whole cell lysate using CIP29 specific antibody. Lane 1 is 1% of twenty million whole cell lysate input and lane 2 is 25% of IP enrichment using rabbit normal IgG (lanes under 'IgG'). Lane 3 is 1% of twenty million whole cell lysate input and lane 4 is 10% IP enrichment using rabbit polyclonal anti-CIP29 antibody (lanes under 'CIP29'). Method: immunoprecipitation Status: Released Lab: Yeo Lab 
Caption: IP-WB analysis of K562 whole cell lysate using the SARNP specific antibody, A303-209A. Lanes 1 and 2 are 2.5% of five million whole cell lysate input and 50% of IP enrichment, respectively, using a normal IgG antibody. Lane 3 is 50% of IP enrichment from five million whole cell lysate using the SARNP-specific antibody, A303-209A. The same antibody was used to detect protein levels via Western blot. This antibody passes preliminary validation and will be further pursued for secondary validation. *NOTE* Protein sizes are taken from Genecards.org and are only estimates based on sequence. Actual protein size may differ based on protein characteristics and electrophoresis method used. Comments: Immunoprecipitation lane (3) exhibits a large deviation from the expected protein size, which we believe is due to performing the characterization using the Jess Western Blotting system. This system has a documented tendency for some proteins to run differently than with more traditional methods due to their compositions and interactions with the electrophoretic components. The image also closely resembles the example image provided by the vendor. Method: immunoprecipitation Status: Released Lab: Yeo Lab | 
Caption: Western blot following CRISPR against SARNP in K562 whole cell lysate using SARNP specific antibody. Lane 1 is a ladder, lane 2 is K562 non-targeting control knockdown, lane 3 and 4 are two different CRISPR against SARNP. SARNP protein appears as the green arrow, Beta-actin serves as a control and appears in red arrow. Releated Sample: BGKcLV33-31 Status: Released Lab: Graveley Lab |
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