Anti-WFS1 antibody [EPR23801-91]
- BOND RX™ Validated
- 20ul selling size
- Recombinant
- Advanced Validation
- RabMAb
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(2 Publications)
Rabbit Recombinant Monoclonal WFS1 antibody. Suitable for mIHC, IHC-P, ICC/IF, IP, WB, IHC-Fr and reacts with Mouse, Rat, Human samples. Cited in 2 publications.
View Alternative Names
Wolframin, Wfs1
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
IHC image of WFS1 staining in a section of frozen normal human pancreas* performed on a Leica BOND™ system using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with ab259362, 1μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HepG2 cells labelling WFS1 with ab259362 at 1/50 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in HepG2 cells is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
IHC image of WFS1 staining in a section of frozen normal human hippocampus* performed on a Leica BOND™ system using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with ab259362, 1μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling WFS1 with ab259362 at 1/5000 dilution (0.093 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : almost no staining on mouse spleen. The section was incubated with ab259362 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- mIHC
Lab
Multiplex immunohistochemistry - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse hippocampus tissue staining SYNPR with ab314136 at a 1 : 8000 (0.06 ug/ml) dilution, WFS1 with ab259362 at 1 : 5000 (0.091 ug/ml) dilution and 5HT6 Receptor with ab315380 at a 1 : 1000 (0.504 ug/ml) dilution followed by secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-SYNPR (yellow; Opal™520), anti-WFS1 (green;Opal™570) and anti-5HT6 Receptor (magenta;Opal™690) on mouse hippocampus.
Panel B : anti-SYNPR staining the mossy fibers in mouse hippocampus.
Panel C : anti-WFS1 staining the pyramidal neurons of CA1 in mouse hippocampus.
Panel D : anti-5HT6 Receptor staining the pyramidal neurons in mouse hippocampus.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab314136, ab259362 and ab315380 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of paraffin-embedded Rat pancreas tissue labelling WFS1 with ab259362 at 1/5000 dilution (0.093 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on rat pancreatic islet. The section was incubated with ab259362 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of paraffin-embedded Mouse pancreas tissue labelling WFS1 with ab259362 at 1/5000 dilution (0.093 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on mouse pancreatic islet (PMID : 15994758). The section was incubated with ab259362 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse pancreas tissue labeling WFS1 with ab259362 at 1/50 (9.28 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse pancreatic islets is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labelling WFS1 with ab259362 at 1/5000 dilution (0.093 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on the CA1 region of rat hippocampus. The section was incubated with ab259362 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling WFS1 with ab259362 at 1/5000 dilution (0.093 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on the CA1 region of mouse hippocampus (PMID : 24694561). The section was incubated with ab259362 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- mIHC
Lab
Multiplex immunohistochemistry - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse hippocampus tissue staining ProDynorphin with ab318966 at a 1 : 5000 (0.1 ug/ml) dilution, SYNPR with ab314136 at 1 : 8000 (0.06 ug/ml) dilution and Wolframin with ab259362 at a 1 : 5000 (0.091 ug/ml) dilution followed by secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-ProDynorphin (magenta; Opal™570), anti-SYNPR (green; Opal™520) and anti-Wolframin (yellow; Opal™690) on mouse hippocampus.
Panel B : anti-ProDynorphin staining the mossy fibers of CA3 in mouse hippocampus.
Panel C : anti-SYNPR staining the mossy fibers of CA3 in mouse hippocampus.
Panel D : anti-Wolframin staining the pyramidal neurons of CA1 in mouse hippocampus.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab318966, ab314136 and ab259362 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat pancreas tissue labeling WFS1 with ab259362 at 1/50 (4.64 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat pancreatic islets is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IP
Supplier Data
Immunoprecipitation - Anti-WFS1 antibody [EPR23801-91] (AB259362)
WFS1 was immunoprecipitated from 0.35 mg Mouse eyeball tissue lysate with ab259362 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab259362 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse eyeball tissue lysate 40 ug
Lane 2 : ab259362 IP in Mouse eyeball tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab259362 in mouse eyeball tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 50 seconds
All lanes:
Immunoprecipitation - Anti-WFS1 antibody [EPR23801-91] (ab259362)
Predicted band size: 100 kDa
Observed band size: 100 kDa,300 kDa
false
- WB
Lab
Western blot - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
The observed MW is consistent with what has been described in the literature (PMID : 12913071).
Lysates were made freshly and used in WB test immediately to minimize protein degradation.
Samples (except lane1) are non-boiled as boiling may cause protein aggregates.
Exposure time : Lane 1 : 10 secondsLane 2-5 : 3 minutes
All lanes:
Western blot - Anti-WFS1 antibody [EPR23801-91] (ab259362) at 1/1000 dilution
Lane 1:
HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
HEK-293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 5:
PC-12 (rat adrenal gland pheochromocytoma) 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 1/50000 dilution
Predicted band size: 100 kDa
Observed band size: 100 kDa,300 kDa
false
- WB
Lab
Western blot - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
The observed MW is consistent with what has been described in the literature (PMID : 12913071 ).
Samples are non-boiled as boiling may cause protein aggregates.
Exposure time : 8 seconds
All lanes:
Western blot - Anti-WFS1 antibody [EPR23801-91] (ab259362) at 1/1000 dilution
All lanes:
Human eyeball tissue lysate at 40 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 100 kDa
Observed band size: 100 kDa,300 kDa
false
- WB
Lab
Western blot - Anti-WFS1 antibody [EPR23801-91] (AB259362)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
The observed MW is consistent with what has been described in the literature (PMID : 12913071).
Low expression : spleen, PC-12 (PMID : 12913071; PMID : 11181571 ).
Samples are non-boiled as boiling may cause protein aggregates.
Exposure time : 8 seconds
All lanes:
Western blot - Anti-WFS1 antibody [EPR23801-91] (ab259362) at 1/1000 dilution
Lane 1:
Mouse eyeball tissue lysate at 40 µg
Lane 2:
Mouse brain tissue lysate at 40 µg
Lane 3:
Mouse spleen tissue lysate at 40 µg
Lane 4:
Rat eyeball tissue lysate at 40 µg
Lane 5:
Rat brain tissue lysate at 40 µg
Lane 6:
PC-12 (rat adrenal gland pheochromocytoma) 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 1/50000 dilution
Predicted band size: 100 kDa
Observed band size: 100 kDa,300 kDa
false
Related conjugates and formulations (2)
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Anti-WFS1 antibody [EPR23801-91] - BSA and Azide free
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-WFS1 antibody [EPR23801-91]
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
This protein plays a role in modulating ER stress responses and calcium homeostasis. It is a part of a signaling complex that influences apoptotic pathways by regulating cellular stress responses. WFS1 affects the stability and function of the ER having an influence over insulin production and secretion. This regulation is important for cells especially those in the pancreatic islets as it affects the secretion of insulin in response to varying glucose levels.
Pathways
WFS1 integrates into the unfolded protein response (UPR) and calcium signaling pathways. These pathways connect to other proteins like ATF6 and PERK which mediate stress-induced responses and adaptations in cells. In the context of insulin regulation the protein contributes to vesicular fusion mechanisms and secretory pathways that facilitate insulin release. WFS1 influences glucose metabolism through direct interactions in pathways regulating cellular stress and protein folding.
Product protocols
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Target data
Publications (2)
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11:e2403405 PubMed39258564
2024
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Cell death and differentiation 31:322-334 PubMed38321214
2024
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Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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