PPP1R8 antibody: RN068PW


Antibody Info
Product_IDRN068PW
Lot_ID1
Host_organismrabbit
SourceMBLI
Antibody_DCC_IDENCAB563YNZ
Target Info
GeneNamePPP1R8
Phosphate
Target_namePPP1R8-human

Validation Images
Cell linePrimary validationSecondary validation
HepG2 PPP1R8-HEPG2-CRISPR.png<br>Caption: Western blot following CRISPR against PPP1R8 in HepG2 whole cell lysate using PPP1R8 specific antibody. Lane 1 is a ladder, lane 2 is HepG2 non-targeting control knockdown, lane 3 and 4 are two different CRISPR against PPP1R8. PPP1R8 protein appears as the green band, GAPDH serves as a control and appears in red.

Caption: Western blot following CRISPR against PPP1R8 in HepG2 whole cell lysate using PPP1R8 specific antibody. Lane 1 is a ladder, lane 2 is HepG2 non-targeting control knockdown, lane 3 and 4 are two different CRISPR against PPP1R8. PPP1R8 protein appears as the green band, GAPDH serves as a control and appears in red.

Releated Sample: BGHcLV12-63

Status: Released

Lab: Graveley Lab

K562 MBL_RN068PW_001_PPP1R8.png<br>Caption: IP-WB analysis of K562 whole cell lysate using the PPP1R8 specific antibody, RN068PW. Lane 1 is 2.5% of five million whole cell lysate input. Lanes 2 and 3 are 50% of IP enrichment from five million whole cell lysate using normal IgG antibody and the PPP1R8-specific antibody, RN068PW. 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.

Caption: IP-WB analysis of K562 whole cell lysate using the PPP1R8 specific antibody, RN068PW. Lane 1 is 2.5% of five million whole cell lysate input. Lanes 2 and 3 are 50% of IP enrichment from five million whole cell lysate using normal IgG antibody and the PPP1R8-specific antibody, RN068PW. 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.

Method: immunoprecipitation

Status: NotSatisfied

Lab: Yeo Lab

PPP1R8_Secondary_Western.png<br>Caption: Western blot following shRNA against PPP1R8 in K562 whole cell lysate using PPP1R8 specific antibody. Lane 1 is a ladder, lane 2 is K562 non-targeting control knockdown, lane 3 and 4 are two different shRNAs against PPP1R8. PPP1R8 protein appears as the green band, Tubulin serves as a control and appears in red.

Caption: Western blot following shRNA against PPP1R8 in K562 whole cell lysate using PPP1R8 specific antibody. Lane 1 is a ladder, lane 2 is K562 non-targeting control knockdown, lane 3 and 4 are two different shRNAs against PPP1R8. PPP1R8 protein appears as the green band, Tubulin serves as a control and appears in red.

Releated Sample: BGKLV28-41

Status: Released

Lab: Graveley Lab