Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate
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ACP1 KO cell lysate available now. KO validated by Next Generation Sequencing, Western blot. Free of charge wild type control included. Knockout achieved by CRISPR/Cas9 X = 1 bp insertion Frameshift = 100%.
View Alternative Names
ACP1, Acid phosphatase 1 soluble, Acid phosphatase of erythrocyte, Adipocyte acid phosphatase, Cytoplasmic phosphotyrosyl protein phosphatase, HAAP, LMW-PTP, LMW-PTPase, Low molecular weight cytosolic acid phosphatase, Low molecular weight phosphotyrosine protein phosphatase, PAP1, PAP2, PPAC_HUMAN, PTPase, Protein tyrosine phosphatase, Purple acid phosphatase, Red cell acid phosphatase 1, phosphatase, acid, of erythrocyte, testicular secretory protein Li 37
- WB
Lab
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate (AB261668)
Lane 1 : Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 2 : ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 3 : K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate 20 ug
Lane 4 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab235448 observed at 18 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab235448 was shown to specifically react with ACP1 (Acid phosphatase 1) in wild-type HEK-293 cells as signal was lost in ACP1 knockout cell line ab261859 (knockout cell lysate ab261668). Wild-type and ACP1 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. ab235448 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Acid phosphatase antibody [EPR21787] (<a href='/en-us/products/primary-antibodies/acid-phosphatase-antibody-epr21787-ab235448'>ab235448</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell line (<a href='/en-us/products/cell-lines/human-acp1-acid-phosphatase-knockout-hek-293-cell-line-ab261859'>ab261859</a>)
Lane 3:
K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate at 20 µg
Lane 4:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Predicted band size: 18 kDa
false
- WB
Lab
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate (AB261668)
Lane 1 : Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 2 : ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 3 : K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate 20 ug
Lane 4 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab166896 observed at 18 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab166896 was shown to recognize ACP1 (Acid phosphatase 1) in wild-type HEK-293 cells as signal was lost at the expected MW in ACP1 knockout cell line ab261859 (knockout cell lysate ab261668). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and ACP1 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. ab166896 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Acid phosphatase/ACP1 antibody [EPR9839] (<a href='/en-us/products/primary-antibodies/acid-phosphatase-acp1-antibody-epr9839-ab166896'>ab166896</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell line (<a href='/en-us/products/cell-lines/human-acp1-acid-phosphatase-knockout-hek-293-cell-line-ab261859'>ab261859</a>)
Lane 3:
K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate at 20 µg
Lane 4:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Predicted band size: 18 kDa
Observed band size: 18 kDa
false
- WB
Lab
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate (AB261668)
Lane 1 : Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 2 : ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 3 : K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate 20 ug
Lane 4 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab180524 observed at 18 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab180524 was shown to specifically react with ACP1 (Acid phosphatase 1) in wild-type HEK-293 cells as signal was lost in ACP1 knockout cell line ab261859 (knockout cell lysate ab261668). Wild-type and ACP1 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. ab180524 and ab8245 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Anti-Acid phosphatase/ACP1 antibody [EPR9838(2)] (<a href='/en-us/products/unavailable/acid-phosphataseacp1-antibody-epr98382-ab180524'>ab180524</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293 whole cell lysate at 20 µg
Lane 2:
ACP1 knockout HEK-293 whole cell lysate at 20 µg
Lane 2:
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell line (<a href='/en-us/products/cell-lines/human-acp1-acid-phosphatase-knockout-hek-293-cell-line-ab261859'>ab261859</a>)
Lane 3:
K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate at 20 µg
Lane 4:
HeLa whole cell lysate at 20 µg
false
- WB
Lab
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate (AB261668)
Lane 1 : Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 2 : ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate 20 ug
Lane 3 : K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate 20 ug
Lane 4 : HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4 : Merged signal (red and green). Green - ab235449 observed at 18 kDa. Red - loading control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37kDa.
ab235449 was shown to react with Acid phosphatase in wild-type HEK-293 cells in western blot with loss of signal observed in ACP1 knockout cell line ab261859 (knockout cell lysate ab261668). Wild-type and ACP1 knockout HEK-293 cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with ab235449 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4°C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Acid phosphatase antibody [EPR21791] (<a href='/en-us/products/primary-antibodies/acid-phosphatase-antibody-epr21791-ab235449'>ab235449</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
ACP1 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
Western blot - Human ACP1 (Acid phosphatase) knockout HEK-293 cell line (<a href='/en-us/products/cell-lines/human-acp1-acid-phosphatase-knockout-hek-293-cell-line-ab261859'>ab261859</a>)
Lane 3:
K562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate at 20 µg
Lane 4:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Predicted band size: 18 kDa
Observed band size: 18 kDa
false
- NGS
Lab
Next Generation Sequencing - Human ACP1 (Acid phosphatase) knockout HEK-293 cell lysate (AB261668)
X = 1 bp insertion
Reactivity data
Product details
Knockout cell lysate achieved by CRISPR/Cas9.
REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.
Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The acid phosphatase enzyme plays an important role in cellular signaling and regulation of metabolic processes. It belongs to the enzyme family of protein tyrosine phosphatases which are key in dephosphorylating proteins and regulating signal transduction pathways. ACP1 does not function as part of a large protein complex but it still affects cellular processes by interacting with multiple molecular partners.
Pathways
The acid phosphatase enzyme is involved in key cellular signaling pathways including the insulin signaling pathway and T-cell receptor signaling. These pathways influence glucose metabolism and immune response. In these pathways ACP1 interacts with proteins such as the insulin receptor substrate and Lck influencing phosphorylation states and cellular activities.
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 2 US: 2
Adherent/suspension
Adherent
Gender
Female
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com