Anti-ZFP36L1 (phospho S92) antibody [EPR19926]
- RabMAb
- Recombinant
- KO Validated
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(1 Publication)
Rabbit Recombinant Monoclonal ZFP36L1 phospho S92 antibody. Suitable for Dot, WB and reacts with Mouse, Human, Synthetic peptide - Human, Transfected cell lysate - Human samples. Cited in 1 publication.
View Alternative Names
BERG36, BRF1, ERF1, RNF162B, TIS11B, ZFP36L1, mRNA decay activator protein ZFP36L1, Butyrate response factor 1, EGF-response factor 1, TPA-induced sequence 11b, ERF-1, ZFP36-like 1
- WB
Lab
Western blot - Anti-ZFP36L1 (phospho S92) antibody [EPR19926] (AB204922)
Blocking and diluting buffer and concentration : 3% NFDM/TBST.
Lysates from the ZFP36L1fl/fl CD4 cre KO mouse were kindly provided by Dr Fiamma Salerno, Turner Lab, Babraham Institute.
Lysates used for the WB were isolated by negative selection using biotinylated abs against Ter119, CD11b, CD11c, Gr1, CD19, B220, F4/80 and NK1.1 to leave a population of CD4 and CD8 positive T cells (the purity of the population was >95% as checked by flow).
Mouse anti-vinculin ab130007, used as the loading control.
All lanes:
Western blot - Anti-ZFP36L1 (phospho S92) antibody [EPR19926] (ab204922) at 1/2500 dilution
Lane 1:
Unstimulated wild-type mouse CD4+ and CD8+ T cells, whole cell lysate (Untreated membrane) at 20 µg
Lane 2:
Wild-type mouse CD4+ and CD8+ T cells treated with 10ng/ml Phorbol-12-myristate-13-acetate (PMA) and 1mM Ionomycin for 3 hours, whole cell lysate (Untreated membrane) at 20 µg
Lane 3:
Unstimulated ZFP36L1 knockout mouse CD4+ and CD8+ T cells, whole cell lysate (Untreated membrane) at 20 µg
Lane 4:
ZFP36L1 knockout mouse CD4+ and CD8+ T cells treated with 10ng/ml Phorbol-12-myristate-13-acetate (PMA) and 1mM Ionomycin for 3 hours, whole cell lysate (Untreated membrane) at 20 µg
Lane 5:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate (Untreated membrane) at 20 µg
Lane 6:
Unstimulated wild-type mouse CD4+ and CD8+ T cells, whole cell lysate (Phosphatase treated membrane) at 20 µg
Lane 7:
Wild-type mouse CD4+ and CD8+ T cells treated with 10ng/ml Phorbol-12-myristate-13-acetate (PMA) and 1mM Ionomycin for 3 hours, whole cell lysate (Phosphatase treated membrane) at 20 µg
Lane 8:
Unstimulated ZFP36L1 knockout mouse CD4+ and CD8+ T cells, whole cell lysate (Phosphatase treated membrane) at 20 µg
Lane 9:
ZFP36L1 knockout mouse CD4+ and CD8+ T cells treated with 10ng/ml Phorbol-12-myristate-13-acetate (PMA) and 1mM Ionomycin for 3 hours, whole cell lysate (Phosphatase treated membrane) at 20 µg
Lane 10:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate, (Phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>); and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-680rd-preadsorbed-ab216776'>ab216776</a>) at 1/15000 dilution
Predicted band size: 36 kDa
Observed band size: 36-47 kDa
false
- WB
Lab
Western blot - Anti-ZFP36L1 (phospho S92) antibody [EPR19926] (AB204922)
Blocking and diluting buffer and concentration : 2% BSA/TBST.
All plasmids were kindly provided by Dr Fiamma Salerno, Turner Lab, Babraham Institute.
The expression profile observed is consistent with what has been described in the literature (PMID : 17030608).
Exposure time : 8 seconds
All lanes:
Western blot - Anti-ZFP36L1 (phospho S92) antibody [EPR19926] (ab204922) at 1/5000 dilution
Lane 1:
HEK-293T (human embryonic kidney epithelial cell) transfected with an empty vector (vector control) containing a myc-His-tag®, whole cell lysate at 10 µg
Lane 2:
HEK-293T transfected with human ZFP36L1 expression vector containing a myc-His-tag®, whole cell lysate at 10 µg
Lane 3:
HEK-293T transfected with human ZFP36L1 expression vector containing a myc-His-tag®, then treated with alkaline phosphatase for 1 hour on the membrane at 10 µg
Lane 4:
HEK-293T transfected with human ZFP36L1 S92A mutant expression vector containing a myc-His-tag®, whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 36 kDa
Observed band size: 36-47 kDa
false
- Dot
Unknown
Dot Blot - Anti-ZFP36L1 (phospho S92) antibody [EPR19926] (AB204922)
Dot blot analysis of ZFP36L1 (phospho S92) labeled with ab204922 at 1/1000 dilution.
Lane 1 : ZFP36L1 (phospho S92) peptide (aa87-97).
Lane 2 : ZFP36L1 non-phospho peptide (aa87-97).
Lane 3 : ZFP36L1 (phospho S125) peptide (aa120-130).
Lane 4 : ZFP36L1 non-phospho peptide (aa120-130).
Blocking and dilution buffer : 5% NFDM/TBST.Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution was used as secondary antibody.
Exposure time : 3 minutes.
Related conjugates and formulations (1)
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Anti-ZFP36L1 (phospho S92) antibody [EPR19926] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
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Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ZFP36L1 acts as a post-transcriptional regulator of gene expression. It destabilizes mRNAs leading to their decay and reduced translation into proteins. While ZFP36L1 often functions as a monomer it can also form complexes with other proteins involved in RNA metabolism. As a result ZFP36L1 plays a critical role in the turnover of pro-inflammatory cytokines and growth factors impacting cellular responses to external stimuli. This regulatory function is essential for maintaining normal cellular homeostasis under various physiological conditions.
Pathways
ZFP36L1 integrates into signaling pathways such as MAPK and NF-kB which are important for inflammation and cellular stress responses. Within these pathways ZFP36L1 interacts with other signaling molecules like MK2 and p38 kinase. These interactions help mediate ZFP36L1's role in mRNA decay influencing the expression of genes involved in the immune response and cell survival. Its participation in these pathways highlights the regulatory landscape in which ZFP36L1 operates affecting diverse cellular functions.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Journal of asthma and allergy 15:529-544 PubMed35515816
2022
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
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