Anti-Glucose Transporter GLUT1 抗体 [EPR3915]

• IHC-P

PubMed

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

GLUT1 and GLUT3 are downregulated in KSHV-infected cells in human KS tumors

Representative illustration of dual immunofluorescence detection of LANA and GLUT1 or in a normal human skin section and a Karposi Sarcoma (KS) tumor section. Tissues were fixed with paraformaldehyhde and paraffin-embedded.

Zhu, Y. et al PLoS Pathog. 2016 May 17;12(5):e1005648. doi: 10.1371/journal.ppat.1005648. eCollection 2016 May Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

• Flow Cyt (Intra)

Lab

Flow Cytometry (Intracellular) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Flow cytometry overlay histogram showing wild-type A549 (green line) and A549-SLC2A1 knockout cells stained with ab115730 (magenta line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10% normal goat serum to block non-specific protein-protein interaction followed by the antibody (ab115730) (1x 10⁶in 100μl at 0.04 μg/ml (1/12500)) for 30min at 22°C.

The secondary antibody Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed was incubated at 1/4000 for 30min at 22°C

Isotype control antibody Recombinant Rabbit IgG, monoclonal [EPR25A] - Isotype Control was used at the same concentration and conditions as the primary antibody (wild-type A549 - black line, A549-SLC2A1 knockout - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity).

Acquisition of >5000 events were collected using a 50 mW Blue laser (488nm) and 525/40 bandpass filter.

This antibody gave a positive signal in A549 WT Fixed with 80% methanol (5 min) / permeabilised with 0.1% PBS-Triton X-100 for 15 min under the same conditions.

• IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 at 1/250 dilution staining Glucose Transporter GLUT1 in Paraffin-embedded human cervical carcinoma tissue by Immunohistochemistry.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing negative staining in human skeletal muscle tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing positive staining in human normal liver tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing positive staining in human urinary bladder transitional carcinoma tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC

Lab

Immunohistochemistry - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunohistochemical analysis of formalin fixed paraffin embedded human placenta labelling Glucose Transporter GLUT1 with ab115730 at a concentration of 0.05µ/ml.

The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with an OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was conducted for 20mins with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5. ab115730 anti-Glucose Transporter GLUT1 was incubated at 37°C for 16mins.

Sections were counterstained is with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.

Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing positive staining in human normal colon tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunohistochemical staining of paraffin embedded human lung carcinoma with purified ab115730 at a working dilution of 1/500. The secondary antibody used is ab97051, a goat anti-rabbit IgG (H&L) at a dilution of 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

• IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 at 1/250 dilution staining Glucose Transporter GLUT1 in Paraffin-embedded human colonic adenocarcinoma tissue by Immunohistochemistry.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• ICC/IF

Lab

Immunocytochemistry/ Immunofluorescence - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

ab115730 staining SLC2A1 in wild-type A549 cells, with negative expression in SLC2A1 knockout A549 cells. The cells were fixed with 100% methanol (5 min), permeabilised with 0.1% Triton x-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated overnight at +4°C with ab115730 at 1 μg/ml and ab7291, Mouse monoclonal [DM1A] to alpha Tubulin at 0.5 μg/ml. Cells were then incubated with ab150081, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 488), pre-adsorbed at 1/1000 dilution (shown in green) and ab150119, Goat polyclonal Secondary Antibody to Mouse IgG - H&L (Alexa Fluor® 647), pre-adsorbed at 1/1000 dilution (shown in red). Nuclear DNA was labelled with DAPI (shown in blue).Image was acquired with a confocal microscope (Leica-Microsystems TCS SP8) and a single confocal section is shown.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing positive staining in human normal breast tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing negative staining in human normal heart tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunofluorescence staining of HepG2 cells with purified ab115730 at a working dilution of 1/100, counter-stained with DAPI. The secondary antibody was Alexa Fluor^® 488 goat anti-rabbit (ab150077), used at a dilution of 1/1000. ab7291, a mouse anti-tubulin antibody (1/1000), was used to stain tubulin along with ab150120 (Alexa Fluor^® 594 goat anti-mouse, 1/1000), shown in the top right hand panel. The cells were fixed in 4% PFA and permeabilized using 0.1% Triton X 100. The negative controls are shown in bottom middle and right hand panels - for negative control 1, purified ab115730 was used at a dilution of 1/500 followed by an Alexa Fluor^® 594 goat anti-mouse antibody (ab150120) at a dilution of 1/500. For negative control 2, ab7291 (mouse anti-tubulin) was used at a dilution of 1/500 followed by an Alexa Fluor^® 488 goat anti-rabbit antibody (ab150077) at a dilution of 1/400.

Alexa Fluor^® 488 (ab195359) and Alexa Fluor^® 647 (ab195020) conjugated versions are available for this clone.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Unpurified ab115730 showing positive staining in human kidney carcinoma tissue.

Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

• IHC

Lab

Immunohistochemistry - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunohistochemical analysis of formalin fixed paraffin embedded human placenta labelling Glucose Transporter GLUT1 with ab115730 at a concentration of 0.2µ/ml. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with a Bond™ Polymer Refine Detection kit. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution 2) for 20mins.

ab115730 anti-Glucose Transporter GLUT1 antibody [EPR3915] was incubated for 15mins at room temperature. Sections were counterstained with Hematoxylin. Image inset shows absence of staining in secondary antibody only control.

Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)

• Flow Cyt (Intra)

Unknown

Flow Cytometry (Intracellular) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Overlay histogram showing HeLa cells stained with unpurified ab115730 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab115730, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor^® 488 goat anti-rabbit IgG (H+L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x10⁶ cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.

• Flow Cyt (Intra)

Unknown

Flow Cytometry (Intracellular) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Overlay histogram showing Jurkat cells fixed in 4% PFA and stained with purified ab115730 at a dilution of 1/40 (red line). The secondary antibody used was Alexa Fluorr^® 488 goat anti-rabbit at a dilution of 1/500. Rabbit monoclonal IgG was used as an isotype control (black line) and cells incubated in the absence of both primary and secondary antibody were used as a negative control (blue line).

Alexa Fluorr^®488 (ab195359) and Alexa Fluorr^®647 (ab195020) conjugated versions are available for this clone.

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunohistochemical staining of paraffin embedded human cervical carcinoma with purified ab115730 at a working dilution of 1/500. The secondary antibody used is ab97051, a goat anti-rabbit IgG (H&L) at a dilution of 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

• WB

Supplier Data

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Lanes 1 - 2 : Merged signal (red and green). Green - ab196357 observed at 54 kDa. Red - loading control, ab8245, observed at 37 kDa.

ab196357 was shown to recognize in wild-type A549 cells as signal was lost at the expected MW in SLC2A1 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and SLC2A1 knockout samples were subjected to SDS-PAGE. ab196357 and ab8245 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1 μg/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1 µg/mL

Lane 1:

Wild-type A549 whole cell lysate at 20 µg

Lane 2:

Western blot - Human SLC2A1 (Glucose Transporter GLUT1) knockout A549 cell line (<a href='/products/cell-lines/human-slc2a1-glucose-transporter-glut1-knockout-a549-cell-line-ab261869'>ab261869</a>) at 20 µg

Lane 2:

Western blot - Human SLC2A1 (Glucose Transporter GLUT1) knockout A549 cell line (<a href='/products/cell-lines/human-slc2a1-glucose-transporter-glut1-knockout-a549-cell-line-ab261869'>ab261869</a>)

Predicted band size: 54 kDa

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• WB

Lab

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Western blot : Anti-Glucose Transporter GLUT1 antibody [EPR3915] staining at 1/100000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab115730 was shown to bind specifically to Glucose Transporter GLUT1. A band was observed at 50-300 kDa in wild-type HepG2 cell lysates with no signal observed at this size in SLC2A1 knockout cell line ab280797 (knockout cell lysate ab284224). To generate this image, wild-type and SLC2A1 knockout HepG2 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3% milk in TBS-0.1% Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4°C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1/100000 dilution

Lane 1:

Wild-type HepG2 cell lysate at 20 µg

Lane 2:

LC2A1 knockout HepG2 cell lysate at 20 µg

Lane 3:

A549 cell lysate at 20 µg

Lane 4:

Jurkat cell lysate at 20 µg

Observed band size: 50-300 kDa

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• WB

Lab

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Blocking buffer : 5% NFDM/TBST
Dilution buffer : 5% NFDM/TBST

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1/1000000 dilution

Lane 1:

HepG2 whole cell lysate at 10 µg

Lane 2:

Human fetal liver lysate at 10 µg

Lane 3:

HT-29 whole cell lysate at 10 µg

Lane 4:

SW480 whole cell lysate at 10 µg

Secondary

All lanes:

Anti-rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution

Predicted band size: 54 kDa

Observed band size: 40-60 kDa

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• WB

Lab

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Exposure time

Lane 1 to 2 : 10 seconds
Lane 3 to 4 : 30 seconds

We recommend not to boil the samples after lysis to get desired WB bands.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1/50000 dilution

Lane 1:

HT-29 (Human colorectal adenocarcinoma epithelial cell) whole cell lysates unboiled at 20 µg

Lane 2:

HT-29 (Human colorectal adenocarcinoma epithelial cell) whole cell lysates boiled at 20 µg

Lane 3:

3T3-L1 (Mouse embryonic fibroblast) whole cell lysates unboiled at 20 µg

Lane 4:

3T3-L1 (Mouse embryonic fibroblast) whole cell lysates boiled at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Predicted band size: 54 kDa

Observed band size: 40-60 kDa

false

• WB

Lab

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1/1000 dilution

All lanes:

Rat placenta tissue lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 40-60 kDa

false

Exposure time: 15s

• IHC-P

PubMed

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Immunohistochemical expression of Glut1 in normal tongue epithelium and tongue cancer. Expression was greatest in lymphocytes (arrows in left upper and lower panels). In the normal oral epithelium, Glut1 was weakly expressed in the basal and spinous cells (left upper panel). In OSCC, Glut1 was upregulated, showing a level of expression comparable with lymphocytes (left and right lower panels). Scale bar, 100 μm.

Note : Glut1 = SLC2A (alternative names for the same target).

Khaom, R. et al PLoS One. 2016 Aug 11;11(8):e0161163. doi: 10.1371/journal.pone.0161163. eCollection 2016 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

• WB

Unknown

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

All lanes:

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (ab115730) at 1/1000 dilution

Lane 1:

Jurkat lysate at 10 µg

Lane 2:

Mouse brain lysate at 10 µg

Lane 3:

Human fetal brain lysate at 10 µg

Lane 4:

3T3L1 lysate at 10 µg

Lane 5:

Human fetal liver lysate at 10 µg

Lane 6:

HepG2 lysate at 10 µg

Predicted band size: 54 kDa

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• OI-RD Scanning

Unknown

OI-RD Scanning - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody. Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.

• WB

CiteAb

Western blot - Anti-Glucose Transporter GLUT1 antibody [EPR3915] (AB115730)

Glucose Transporter GLUT1 Western Blotting using Anti-Glucose Transporter GLUT1 antibody [EPR3915], ab115730. Publication image from Yang, Q. et al., 2018, Nat Commun, PubMed : 30405100.

PRKAA1 is required for disturbed flow-induced metabolic alteration of ECs. a–c Representative images and quantification data of en face immunofluorescence staining for Slc2a1 and Pfkfb3 (red) on arterial endothelium of Prkaa1f/f and Prkaa1VEC-KO mice. The endothelium was visualized by CD31 staining (Alexa Fluor-488, green). Nuclei were counterstained with DAPI (blue). Images were captured with confocal fluorescent microscopy. Scale bar : 20 µm; n = 7. d Real-time PCR analysis of mRNA levels of glycolytic genes (Hif1a, Slc2a1, Pfkfb3, Hk1, and Ldha) of ECs from sham-operated right carotid arteries in Prkaa1f/f mice and partially ligated left carotid arteries in Prkaa1f/f and Prkaa1VEC-KO mice. n = 9 mice per group. e Real-time PCR analysis of mRNA levels of HIF1A, SLC2A1, PFKFB3, and HK1 in HUVECs transfected with siCtrl and siPRKAA1 under laminar flow and oscillating flow for 24 h. n = 4. f Western-blot analysis and quantification data of protein levels of HIF1A, SLC2A1, and PFKFB3 in HUVECs transfected with siCtrl and siPRKAA1 under laminar flow and oscillating flow for 24 h. n = 4. g Western-blot analysis and quantification data of protein level of Cezanne in HUVECs transfected with siCtrl and siPRKAA1 under laminar flow and oscillating flow for 24 h. n = 4. h Western-blot analysis and quantification data of protein levels of p-PRKA, PRKAA1, PRKAA, SLC2A1, and PFKFB3 in HUVECs transfected with siCtrl and siHIF1A under laminar flow and oscillating flow for 24 h. n = 4. i Western-blot analysis and quantification data of protein levels of SLC2A1 and PFKFB3 in HUVECs transfected with siCtrl-Ad-Ctrl, siPRKAA1-Ad-Ctrl, and siPRKAA1-Ad-HIF1A under oscillating flow for 24 h. n = 5. All data were expressed as mean ± SEM. Statistical significance was determined by one-way ANOVA followed by Bonferroni test. *p < 0.05 was considered significant, **p < 0.01, ***p < 0.001

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