Anti-WIPI2 (phospho S413) antibody [EPR27037-149]
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
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Knockout Tested Rabbit Recombinant Monoclonal WIPI2 phospho S413 antibody. Suitable for Dot, WB and reacts with Synthetic peptide - Mouse, Human, Mouse, Rat samples.
View Alternative Names
WD repeat domain phosphoinositide-interacting protein 2, WIPI-2, Wipi2
- WB
Supplier Data
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The identity of the higher MW band at approximately 250kDa is unknown In Western blot, anti-WIPI2 antibody (ab105459) staining at 1/1000 dilution.Anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (ab310325) at 1/1000 dilution
Lane 1:
Untreated wild-type HAP1(human chronic myelogenous leukemia near-haploid cell line) whole cell lysate at 20 µg
Lane 2:
HAP1 treated with 200 nM TPA for 30 min, whole cell lysate at 20 µg
Lane 3:
WIPI2 knockout HAP1 whole cell lysate
Lane 4:
WIPI2 knockout HAP1 treated with 200 nM TPA for 30 min, whole cell lysate at 20 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
Observed band size: 50 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The identity of the higher MW band at approximately 250kDa is unknown. In Western blot, anti-WIPI2 antibody (ab105459) staining at 1/1000 dilution.Anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (ab310325) at 1/1000 dilution
Lane 1:
Untreated KARPAS-299 (human T cell lymphoma cell) starved overnight whole cell lysate (untreated membrane) at 20 µg
Lane 2:
KARPAS-299 starved overnight, then treated with 200nM TPA for 30min whole cell lysate (untreated membrane) at 20 µg
Lane 3:
Untreated KARPAS-299 starved overnight whole cell lysate (phosphatase treated membrane) at 20 µg
Lane 4:
KARPAS-299 starved overnight, then treated with 200nM TPA for 30min whole cell lysate (phosphatase treated membrane) at 20 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
Observed band size: 50 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The identity of the higher MW band at approximately 250kDa is unknown In Western blot, anti-WIPI2 antibody (ab105459) staining at 1/1000 dilution.Anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (ab310325) at 1/1000 dilution
Lane 1:
Untreated Raji (human Burkitts lymphoma B lymphocyte) whole cell lysate
Lane 2:
Raji starved overnight, then treated with 200nM TPA for 30min whole cell lysate
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
Observed band size: 50 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The identity of the higher MW band at approximately 250kDa is unknown. In Western blot, anti-WIPI2 antibody (ab105459) staining at 1/1000 dilution.Anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (ab310325) at 1/1000 dilution
Lane 1:
Untreated MEF (mouse embryonic fibroblast (immortalized)) whole cell lysate at 20 µg
Lane 2:
MEF treated with 5uM MG-132 for 6h whole cell lysate at 20 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
Observed band size: 50 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Low expression : liver tissue(PMID : 15602573) The identity of the higher MW band at approximately 250kDa is unknown. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (ab310325) at 1/1000 dilution
Lane 1:
Rat testis tissue lysate at 20 µg
Lane 2:
Rat liver tissue lysate at 20 µg
Lane 3:
Mouse testis tissue lysate at 20 µg
Lane 4:
Mouse liver tissue lysate at 20 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
Observed band size: 50 kDa
false
Exposure time: 180s
- Dot
Supplier Data
Dot Blot - Anti-WIPI2 (phospho S413) antibody [EPR27037-149] (AB310325)
Dot blot analysis of WIPI2 (phospho S413) using ab310325 at 1 : 1000 (0.499 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution. Lane 1 : Mouse WIPI2 phospho (S395) peptide a Lane 2 : Mouse WIPI2 phospho (S395) peptide b Lane 3 : Mouse WIPI2 non-phospho peptide Exposure time : 180 seconds Blocking and diluting buffer and concentration : 5% NFDM/TBST
Related conjugates and formulations (1)
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Anti-WIPI2 (phospho S413) antibody [EPR27037-149] - 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
Form
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
WIPI2 serves as an important scaffold in the formation of the autophagy machinery. It is part of a larger complex that includes key proteins like Atg16L1 and ULK1 which are essential in the autophagy process. WIPI2 assists in recruiting additional autophagic factors to the developing autophagosome contributing to the membrane curvature and expansion necessary for cargo sequestration. Its activity ensures the efficient turnover of damaged organelles and proteins maintaining cellular health and homeostasis.
Pathways
WIPI2 integrates into the autophagy and PI3K/Akt signaling pathways. Each of these pathways plays a significant role in cellular response to nutrient deprivation and stress. In the autophagy pathway WIPI2 directly interacts with proteins like LC3 facilitating the biogenesis of autophagosomes. Through the PI3K/Akt pathway WIPI2 supports cell survival and growth regulation linking metabolic status with autophagic responses. This interaction highlights its importance in cellular adaptation to environmental changes.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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