AKAP1 antibody: A301-062A


Antibody Info
Product_IDA301-062A
Lot_ID1
Host_organismrabbit
SourceBethyl Labs
Antibody_DCC_IDENCAB322CRJ
Target Info
GeneNameAKAP8
Phosphate
Target_nameAKAP8-human
Antibody Info
Product_IDA301-062A
Lot_ID1
Host_organismrabbit
SourceBethyl Labs
Antibody_DCC_ID
Target Info
GeneNameAKAP1
PhosphateENCAB322CR
Target_nameAKAP1phosphoAB322CR-human

Validation Images
Cell linePrimary validationSecondary validation
K562 Bethyl_A301-062A_1_AKAP8.png<br>Caption: IP-WB analysis of K562 whole cell lysate using the AKAP8 specific antibody, A301-062A. 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 AKAP8-specific antibody, A301-062A. 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 AKAP8 specific antibody, A301-062A. 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 AKAP8-specific antibody, A301-062A. 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

Cell linePrimary validationSecondary validation
K562 AKAP1-K562-A301-062A.png<br>Caption: Western blot following shRNA against AKAP1-ENCAB322CR in K562 whole cell lysate using AKAP1-ENCAB322CR specific antibody. Lane 1 is a ladder, lane 2 is K562 non-targeting control knockdown, lane 3 and 4 are two different shRNA against AKAP1-ENCAB322CR. AKAP1-ENCAB322CR protein appears as the green arrow, Beta-actin serves as a control and appears in red arrow.

Caption: Western blot following shRNA against AKAP1-ENCAB322CR in K562 whole cell lysate using AKAP1-ENCAB322CR specific antibody. Lane 1 is a ladder, lane 2 is K562 non-targeting control knockdown, lane 3 and 4 are two different shRNA against AKAP1-ENCAB322CR. AKAP1-ENCAB322CR protein appears as the green arrow, Beta-actin serves as a control and appears in red arrow.

Releated Sample: BGKLV32-7

Status: Experimented

Lab: Graveley Lab