Rabbit Recombinant Monoclonal Integrin alpha V antibody. Suitable for IP, WB, ICC/IF, IHC-P and reacts with Human, Mouse, Rat samples. Cited in 73 publications.
IgG
Rabbit
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Liquid
Monoclonal
IP | WB | ICC/IF | IHC-P | |
---|---|---|---|---|
Human | Tested | Tested | Tested | Tested |
Mouse | Expected | Tested | Expected | Tested |
Rat | Expected | Tested | Expected | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/40 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/5000 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/5000 | Notes - |
Species Human | Dilution info 1/5000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/500 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Human | Dilution info 1/500 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
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The alpha-V (ITGAV) integrins are receptors for vitronectin, cytotactin, fibronectin, fibrinogen, laminin, matrix metalloproteinase-2, osteopontin, osteomodulin, prothrombin, thrombospondin and vWF. They recognize the sequence R-G-D in a wide array of ligands. ITGAV:ITGB3 binds to fractalkine (CX3CL1) and may act as its coreceptor in CX3CR1-dependent fractalkine signaling (PubMed:23125415). ITGAV:ITGB3 binds to NRG1 (via EGF domain) and this binding is essential for NRG1-ERBB signaling (PubMed:20682778). ITGAV:ITGB3 binds to FGF1 and this binding is essential for FGF1 signaling (PubMed:18441324). ITGAV:ITGB3 binds to FGF2 and this binding is essential for FGF2 signaling (PubMed:28302677). ITGAV:ITGB3 binds to IGF1 and this binding is essential for IGF1 signaling (PubMed:19578119). ITGAV:ITGB3 binds to IGF2 and this binding is essential for IGF2 signaling (PubMed:28873464). ITGAV:ITGB3 binds to IL1B and this binding is essential for IL1B signaling (PubMed:29030430). ITGAV:ITGB3 binds to PLA2G2A via a site (site 2) which is distinct from the classical ligand-binding site (site 1) and this induces integrin conformational changes and enhanced ligand binding to site 1 (PubMed:18635536, PubMed:25398877). ITGAV:ITGB3 and ITGAV:ITGB6 act as a receptor for fibrillin-1 (FBN1) and mediate R-G-D-dependent cell adhesion to FBN1 (PubMed:12807887, PubMed:17158881). Integrin alpha-V/beta-6 or alpha-V/beta-8 (ITGAV:ITGB6 or ITGAV:ITGB8) mediates R-G-D-dependent release of transforming growth factor beta-1 (TGF-beta-1) from regulatory Latency-associated peptide (LAP), thereby playing a key role in TGF-beta-1 activation (PubMed:15184403, PubMed:22278742, PubMed:28117447). ITGAV:ITGB3 act as a receptor for CD40LG (PubMed:31331973).(Microbial infection) Integrin ITGAV:ITGB5 acts as a receptor for Adenovirus type C.(Microbial infection) Integrin ITGAV:ITGB5 and ITGAV:ITGB3 act as receptors for Coxsackievirus A9 and B1.(Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for Herpes virus 8/HHV-8.(Microbial infection) Integrin ITGAV:ITGB6 acts as a receptor for herpes simplex 1/HHV-1.(Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for Human parechovirus 1.(Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for West nile virus.(Microbial infection) In case of HIV-1 infection, the interaction with extracellular viral Tat protein seems to enhance angiogenesis in Kaposi's sarcoma lesions.
Integrin alpha-V, Vitronectin receptor, Vitronectin receptor subunit alpha, VNRA, MSK8, VTNR, ITGAV
Rabbit Recombinant Monoclonal Integrin alpha V antibody. Suitable for IP, WB, ICC/IF, IHC-P and reacts with Human, Mouse, Rat samples. Cited in 73 publications.
Integrin alpha-V, Vitronectin receptor, Vitronectin receptor subunit alpha, VNRA, MSK8, VTNR, ITGAV
IgG
Rabbit
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Liquid
Monoclonal
EPR16800
Affinity purification Protein A
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
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.
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/1000 dilution
Lane 1: Untreated HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate. at 15 µg
Lane 2: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate treated with PNGase F. at 15 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 116 kDa
Observed band size: 116.135 kDa
Exposure time: 20s
Integrin alpha V was immunoprecipitated from 1 mg of A549 (Human lung carcinoma) whole cell extract with ab179475 at 1/40 dilution. Western blot analysis was performed from the immunoprecipitate using ab179475 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
Lane 1: A549 whole cell extract.
Lane 2: PBS instead of A549 whole cell extract.
Blocking/Dilution buffer: 5% NFDM/TBST.
ab179475 can recognize 135kDa full length Integrin alpha V and 125kDa heavy chain. The 125 kDa band is Integrin alpha V heavy chain.
All lanes: Immunoprecipitation - Anti-Integrin alpha V antibody [EPR16800] (ab179475)
Predicted band size: 116 kDa
Observed band size: 125 kDa
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/1000 dilution
Lane 1: Untreated K-562 (Human chronic myelogenous leukemia lymphoblast) whole cell lysate. at 15 µg
Lane 2: K-562 (Human chronic myelogenous leukemia lymphoblast) treated with PNGase F whole cell lysate. at 15 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 116 kDa
Observed band size: 116.135 kDa
Exposure time: 80s
Blocking/dilution buffer: 5% NFDM/TBST.
ab179475 can recognize 135kDa full length Integrin alpha V and 125kDa heavy chain. The 125 kDa band is Integrin alpha V heavy chain.
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/50000 dilution
Lane 1: HUVEC (Human umbilical vein endothelial cell line) whole cell lysates at 20 µg
Lane 2: HT-29 (Human colorectal adenocarcinoma cells) whole cell lysates at 20 µg
Lane 3: A549 (Human lung carcinoma) whole cell lysates at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 116 kDa
Observed band size: 125 kDa
Diluent: 2% BSA in 1X TBST.
Blocked using 5% BSA for 1 hour at RT.
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/2000 dilution
All lanes: Mouse skin whole cell lysate at 40 µg
All lanes: Goat anti-Rabbit IgG(H+L)-HRP at 1/5000 dilution
Developed using the ECL technique.
Predicted band size: 116 kDa
Exposure time: 25s
Immunohistochemical analysis of paraffin-embedded human transitional cell carcinoma of bladder tissue labeling Integrin alpha V with ab179475 at 1/500 dilution followed by Goat Anti-Rabbit HRP (IgG H&L) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution.
Membrane and weak cytoplasm staining on human transitional cell carcinoma of bladder is observed. Counterstained with hematoxylin.
Negative control: Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized A549 (Human lung carcinoma) cells labeling Integrin alpha V with ab179475 at 1/500 dilution, followed by Goat anti-rabbit Alexa Fluor® 488 (IgG) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/400 dilution (green).
Confocal image showing membrane and cytoplasm staining on A549 cell line. The nuclear counterstain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (goat anti-mouse AlexaFluor®594 secondary antibody) at 1/500 dilution (red).
The negative controls are as follows:
-ve control 1: ab179475 at 1/500 dilution followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2: Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/400 dilution.
Blocking/dilution buffer: 5% NFDM/TBST.
ab179475 can recognize 135kDa full length Integrin alpha V and 125kDa heavy chain. The 125 kDa band is Integrin alpha V heavy chain.
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/5000 dilution
Lane 1: Human fetal kidney lysates at 10 µg
Lane 2: Human fetal brain lysates at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 116 kDa
Observed band size: 125 kDa
Immunohistochemical analysis of paraffin-embedded human kidney tissue labeling Integrin alpha V with ab179475 at 1/500 dilution followed by Goat Anti-Rabbit HRP (IgG H&L) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution.
Membrane and cytoplasm staining on human kidney tubules is observed. Counterstained with hematoxylin.
Negative control: Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Blocking/dilution buffer: 5% NFDM/TBST.
ab179475 can recognize 135kDa full length Integrin alpha V and 125kDa heavy chain. The 125 kDa band is Integrin alpha V heavy chain.
All lanes: Western blot - Anti-Integrin alpha V antibody [EPR16800] (ab179475) at 1/5000 dilution
Lane 1: Mouse brain lysates at 10 µg
Lane 2: Mouse kidney lysates at 10 µg
Lane 3: Mouse spleen lysates at 10 µg
Lane 4: Rat brain lysates at 10 µg
Lane 5: Rat kidney lysates at 10 µg
Lane 6: C6 (Rat glial tumor cells) whole cell lysates at 10 µg
Lane 7: NIH/3T3 (Mouse embyro fibroblast cells) whole cell lysates at 10 µg
Lane 8: Raji (Human Burkitt's lymphoma cell line) whole cell lysates at 10 µg
All lanes: Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 116 kDa
Observed band size: 125 kDa, 135 kDa
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue labeling Integrin alpha V with ab179475 at 1/500 dilution followed by Goat Anti-Rabbit HRP (IgG H&L) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary at 1/500 dilution.
Membrane and cytoplasm staining on mouse kidney tubule and glomerulus is observed. Counterstained with hematoxylin.
Negative control: Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 and ab179475 were used as loading controls.
The molecular weight observed is consistent with literatures (PMID: 9722601, PMID: 3360311).
Samples are non-boiled as boiling may cause protein aggregation and were run on a Bis-Tris gel.
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/200000 dilution and anti- Integrin alpha V antibody (ab179475) loading control staining at 1/5000 dilution.
All lanes: Western blot - Anti-CaSR antibody [EPR24050-59] (Anti-CaSR antibody [EPR24050-59] ab259846) at 1/1000 dilution
Lane 1: Mouse kidney membrane tissue lysate at 10 µg
Lane 2: Mouse kidney membrane control tissue lysate at 10 µg
Lane 3: Rat kidney membrane tissue lysate at 10 µg
Lane 4: Rat skeletal muscle tissue lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Exposure time: 10s
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
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-HMGA1 antibody [RM1061] (Anti-HMGA1 antibody [RM1061] ab315350) at 1/1000 dilution
Lane 1: BxPC-3 (human pancreas adenocarcinoma epithelial cell) nuclear fraction at 20 µg
Lane 2: BxPC-3 (human pancreas adenocarcinoma epithelial cell) cytoplasmic fraction at 20 µg
Lane 3: BxPC-3 (human pancreas adenocarcinoma epithelial cell) membrane fraction at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 17 kDa, 36 kDa, 15 kDa, 125 kDa
Exposure time: 92s
Low expression: HL-1.
Lysates were freshly made and used for Western blotting immediately to minimize protein degradation.
Alternatively spliced forms of the EVI-1 gene encode at least three distinct proteins: EVI-1 (145 kDa), MDS1/EVI-1 (200 kDa) and EVI-1Δ324 (88 kDa) PMID:(PMID: 24944602).
The identity of the bands between 75 kDa and 180 kDa are unknown.
In Western blot, Anti-Integrin alpha V antibody [EPR16800] (ab179475) staining at 1/5000 dilution.
All lanes: Western blot - Anti-EVI1 antibody [EPR26816-18] (Anti-EVI1 antibody [EPR26816-18] ab315973) at 1/1000 dilution
Lane 1: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 80 µg
Lane 2: HL-1 (mouse atrial muscle cell) whole cell lysate at 80 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 200 kDa, 125 kDa
Exposure time: 59s
The identity of the higher MW band at approximately 50 kDa (in lane 2) is unknown.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade ab176842) staining at 1/100000 dilution.
In Western blot, Anti-Integrin alpha V antibody [EPR16800] (ab179475) staining at 1/5000 dilution.
All lanes: Western blot - Anti-GPCR GPRC5D antibody [EPR28376-41] (Anti-GPCR GPRC5D antibody [EPR28376-41] ab315808) at 1/1000 dilution
Lane 1: RPMI-8226 (human plasmacytoma, myeloma B lymphocyte) membrane fraction at 50 µg
Lane 2: RPMI-8226 nuclear fraction at 50 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 33 kDa, 125 kDa, 15 kDa
Exposure time: 15s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The identity of the bands between 75 kDa and 25 kDa are unknown.
In Western blot, Anti-Vinculin antibody [EPR8185] (Anti-Vinculin antibody [EPR8185] ab129002) staining at 1/10000 dilution.
In Western blot, Anti-Integrin alpha V antibody [EPR16800] (ab179475) staining at 1/5000 dilution.
All lanes: Western blot - Anti-GluN2D antibody [EPR28378-56] (Anti-GluN2D antibody [EPR28378-56] ab314664) at 1/1000 dilution
Lane 1: Mouse brain tissue lysate at 20 µg
Lane 2: Mouse brain membrane fraction at 20 µg
Lane 3: Mouse brain non-membrane fraction at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 165 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
This blot was developed using a high sensitivity ECL substrate.
Exposure time: 3 minutes
All lanes: Western blot - Anti-RANK antibody [EPR26196-15] (Anti-RANK antibody [EPR26196-15] ab305233) at 1/1000 dilution
Lane 1: K-562 (human chronic myelogenous leukemia lymphoblast) non-membrane fraction at 20 µg
Lane 2: K-562 membrane fraction at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Developed using the ECL technique.
Observed band size: 80 kDa
Exposure time: 3min
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The molecular weight observed is consistent with what has been described in the literature (PMID: 29285063, 19726871).
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/200000 dilution. Anti-Integrin alpha V (ab179475) control staining at 1/5000 dilution
Exposure time: 37 seconds
All lanes: Western blot - Anti-Cx40/GJA5 antibody [EPR28370-62] (Anti-Cx40/GJA5 antibody [EPR28370-62] ab313644) at 1/1000 dilution
Lane 1: Mouse lung non-membrane fraction at 20 µg
Lane 2: Mouse lung membrane fraction 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: 40, 36 kDa
Exposure time: 37s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Negative controls: kidney (PMID: 24309898), cerebellum (PMID: 24309898).
In Western blot, anti- Integrin alpha V antibody (ab179475) loading control staining at 1/5000 dilution.
Exposure time: 180 seconds
All lanes: Western blot - Anti-Neutrophil Elastase antibody [EPR28386-66] (Anti-Neutrophil Elastase antibody [EPR28386-66] ab310335) at 1/1000 dilution
Lane 1: Rat bone marrow tissue lysate at 20 µg
Lane 2: Rat cerebellum tissue lysate at 20 µg
Lane 3: Rat kidney tissue lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Kir4.1/KCNJ10 is expressed in vivo as a homotetramer (four units of KIR4.1) or a heterotetramer with KIR5.1(two units of KIR4.1 and KIR5.1). (PMID: 33348803; PMID: 15310750 ). This antibody can only detect the tetramer of Kir4.1/KCNJ10.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/200000 dilution. Anti-Integrin alpha V (ab179475) control staining at 1/1000 dilution
Exposure time: 15 seconds
All lanes: Western blot - Anti-Kir4.1/KCNJ10 antibody [EPR27251-74] (Anti-Kir4.1/KCNJ10 antibody [EPR27251-74] ab312844) at 1/1000 dilution
Lane 1: Mouse brain non-membrane fraction at 20 µg
Lane 2: Mouse brain membrane fraction at 20 µg
Lane 3: Rat brain non-membrane fraction at 20 µg
Lane 4: Rat brain membrane fraction 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: 250 kDa
Exposure time: 15s
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200, 000 dilution and anti-Integrin alpha V (ab179475) staining at 1/5, 000 dilution.
Samples are non-boiled as boiling may cause protein aggregation.
All lanes: Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] (Anti-Noradrenaline transporter antibody [EPR23527-534] ab254361) at 1/1000 dilution
Lane 1: Mouse brain membrane tissue lysate at 20 µg
Lane 2: Mouse brain membrane control tissue lysate at 20 µg
Lane 3: Rat brain membrane tissue lysate at 20 µg
Lane 4: Rat brain membrane control 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
Predicted band size: 69 kDa
Observed band size: 69 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The identity of the bands higher than 150 kDa and lower than 50 kDa are unknown.
In Western blot, Anti-Integrin alpha V antibody [EPR16800] (ab179475) staining at 1/5000 dilution.
All lanes: Western blot - Anti-FRS2 antibody [EPR28714-126] (Anti-FRS2 antibody [EPR28714-126] ab320727) at 1/1000 dilution
Lane 1: F9 (mouse embryonal carcinoma epithelial cell) non-membrane fraction at 20 µg
Lane 2: F9 (mouse embryonal carcinoma epithelial cell) membrane fraction at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 74 kDa, 116 kDa, 135 kDa
Exposure time: 180s
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