Rabbit Recombinant Multiclonal Aquaporin 5 antibody. Carrier free. Suitable for WB, IHC-P, IP, ICC/IF, IHC-Fr and reacts with Human, Mouse, Rat samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Multiclonal
WB | IHC-P | IP | ICC/IF | IHC-Fr | Flow Cyt | |
---|---|---|---|---|---|---|
Human | Tested | Tested | Tested | Tested | Expected | Not recommended |
Mouse | Tested | Tested | Tested | Not recommended | Tested | Not recommended |
Rat | Tested | Tested | Tested | Not recommended | Tested | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Select an associated product type
Aquaporins form homotetrameric transmembrane channels, with each monomer independently mediating water transport across the plasma membrane along its osmotic gradient (PubMed:18768791, PubMed:8621489). Plays an important role in fluid secretion in salivary glands (By similarity). Required for TRPV4 activation by hypotonicity. Together with TRPV4, controls regulatory volume decrease in salivary epithelial cells (PubMed:16571723). Seems to play a redundant role in water transport in the eye, lung and in sweat glands (By similarity).
Aquaporin-5, AQP-5, AQP5
Rabbit Recombinant Multiclonal Aquaporin 5 antibody. Carrier free. Suitable for WB, IHC-P, IP, ICC/IF, IHC-Fr and reacts with Human, Mouse, Rat samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Multiclonal
Yes
RM1099
Affinity purification Protein A
Unsuitable for mouse and rat ICC.
Blue Ice
+4°C
+4°C
ab315856 is the carrier-free version of Anti-Aquaporin 5 antibody [RM1099] ab315855.
This product is a recombinant multiclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This supplementary information is collated from multiple sources and compiled automatically.
The protein known as Aquaporin 5 often abbreviated as AQP5 is a member of the aquaporin family which are integral membrane proteins that function as channels for water. This particular protein facilitates water transport across cell membranes an action critical in maintaining fluid balance. Aquaporin 5 has a molecular mass of approximately 29 kDa. It is largely expressed in epithelial cells in various tissues including the salivary glands lacrimal glands and respiratory tissues. It is recognized by different names such as Aquaporin-5 and sometimes referenced in studies as Aquazol 5.
Water transport and secretion processes heavily rely on the presence of Aquaporin 5. It is integral in the formation of tight junctions in epithelial cells enhancing cell permeability to water. Unlike some other aquaporins Aquaporin 5 operates independently and is not known to be part of a larger protein complex. Its presence influences the efficiency of fluid secretion affecting activities such as salivation and tear secretion. The capacity of AQP5 to control water movement tightly connects it to cellular hydration homeostasis.
Aquaporin 5 is significantly involved in the regulation of water balance and osmotic equilibrium in epithelial tissues. Its role in fluid secretion pathways is interconnected with other proteins like Aquaporin 4 which share similar duties in the osmotic control of water. In the water transport pathways AQP5 coordinates with proteins like CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) to manage fluid movement particularly in the respiratory passages and glands. The precise regulation of water flow by these pathways ensures that overall tissue hydration remains constant.
Aquaporin 5 is directly associated with conditions such as Sjögren's syndrome and xerostomia (dry mouth syndrome). During Sjögren's syndrome malfunction of AQP5 can lead to impaired salivary and tear secretion contributing to the symptoms of dryness. Furthermore defects or polymorphisms in AQP5 have implications in respiratory diseases potentially affecting proteins like Aquaporin 3 which shares functional similarities. Understanding the role of AQP5 in these conditions enables further exploration into therapeutic targets and treatment methods.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Vinculin antibody [EPR8185] (Anti-Vinculin antibody [EPR8185] ab129002) staining at 1/10000 dilution.
All lanes: Western blot - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/1000 dilution
Lane 1: Mouse lung tissue lysate at 20 µg
Lane 2: Mouse kidney tissue lysate at 20 µg
Lane 3: Mouse heart tissue lysate at 20 µg
Lane 4: Rat lung tissue lysate at 20 µg
Lane 5: Rat kidney tissue lysate at 20 µg
Lane 6: Rat salivary tissue lysate at 20 µg
Lane 7: Rat heart tissue lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 24 kDa, 124 kDa
Exposure time: 15s
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Vinculin antibody [EPR8185] (Anti-Vinculin antibody [EPR8185] ab129002) staining at 1/10000 dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Aquaporin 5 was immunoprecipitated from 0.35 mg Rat lung tissue lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Rat lung tissue lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in Rat lung tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in rat lung tissue lysate
All lanes: Immunoprecipitation - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/30 dilution
All lanes: Rat lung tissue lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/1000 dilution
Aquaporin 5 was immunoprecipitated from 0.35 mg Rat lung tissue lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Rat lung tissue lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in Rat lung tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in rat lung tissue lysate
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Aquaporin 5 was immunoprecipitated from 0.35 mg Mouse lung tissue lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Mouse lung tissue lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in Mouse lung tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in mouse lung tissue lysate
All lanes: Immunoprecipitation - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/30 dilution
All lanes: Mouse lung tissue lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/1000 dilution
Exposure time: 24s
Aquaporin 5 was immunoprecipitated from 0.35 mg Mouse lung tissue lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Mouse lung tissue lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in Mouse lung tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in mouse lung tissue lysate
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Aquaporin 5 was immunoprecipitated from 0.35 mg KATO III (human stomach spherical) whole cell lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: KATO III (human stomach spherical) whole cell lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in KATO III (human stomach spherical) whole cell lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in KATO III whole cell lysate lysate
All lanes: Immunoprecipitation - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/30 dilution
All lanes: KATO III (human stomach spherical) whole cell lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/1000 dilution
Exposure time: 24s
Aquaporin 5 was immunoprecipitated from 0.35 mg KATO III (human stomach spherical) whole cell lysate with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: KATO III (human stomach spherical) whole cell lysate
Lane 2: Anti-Aquaporin 5 antibody [RM1099] ab315855 IP in KATO III (human stomach spherical) whole cell lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Aquaporin 5 antibody [RM1099] ab315855 in KATO III whole cell lysate lysate
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
All lanes: Western blot - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/5000 dilution
Lane 1: KATO III (human stomach spherical) whole cell lysate at 10 µg
Lane 2: K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 24 kDa, 36 kDa
Exposure time: 10s
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse lung. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
All lanes: Western blot - Anti-Aquaporin 5 antibody [RM1099] (Anti-Aquaporin 5 antibody [RM1099] ab315855) at 1/1000 dilution
Lane 1: Human salivary grand tissue lysate at 20 µg
Lane 2: Human liver tissue lysate at 20 µg
Lane 3: Human skeletal muscle tissue lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 24 kDa, 36 kDa
Exposure time: 15s
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat kidney (fresh frozen) tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/500 (0.984 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Low expression: confocal image showing no staining on rat kidney (PMID: 9767520). The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse kidney (fresh frozen) tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/500 (0.984 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Low expression: confocal image showing no staining on mouse kidney (PMID: 9767520). The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat lung (fresh frozen) tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/500 (0.984 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Confocal image showing positive staining on rat lung. The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse lung (fresh frozen) tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/500 (0.984 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Confocal image showing positive staining on mouse lung. The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on rat cardiac muscle. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on mouse cardiac muscle. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on mouse skeletal muscle. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on human skeletal muscle. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat salivary gland tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat salivary gland. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat lung tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat lung. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse salivary gland tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse salivary gland. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human salivary gland tissue labeling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human salivary gland. The section was incubated with Anti-Aquaporin 5 antibody [RM1099] ab315855 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
This data was developed using Anti-Aquaporin 5 antibody [RM1099] ab315855, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized KATO III (human stomach spherical cell) cells labelling Aquaporin 5 with Anti-Aquaporin 5 antibody [RM1099] ab315855 at 1/100 (4.92 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green).
Confocal image showing membranous and cytoplasmic staining in KATO III cell line.
Negative control: K-562.
Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).
Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/500 1ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/ml dilution.
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