Fig1: Western blot analysis of GLUT1 on different cell lysates using anti-GLUT1 antibody at 1/1000 dilution. Positive control: Lane 1: Hela Lane 2: MCF-7 Lane 3: Jurkat Lane 4: NIH/3T3
Fig2: ICC staining GLUT1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: ICC staining GLUT1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig4: ICC staining GLUT1 in HepG2 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig5: Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig6: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig7: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig8: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig9: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig10: Flow cytometric analysis of Hela cells with GLUT1 antibody at 1/50 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody
Product Name | Glucose Transporter GLUT1 [SA0377] |
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Antibody Type | Primary Antibodies |
Product description |
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Immunogen | recombinant protein |
Clonality | Monoclonal |
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Isotype | IgG |
Host Species | Recombinant rabbit |
Tested Applications | |
WB:1:500-1:1,000 ICC:1:50-1:200 IHC:1:50-1:200 FC:1:10-1:100 |
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Species Reactivity | |
Concentration | 1 mg/mL. |
Alternative Names | Choreoathetosis/spasticity episodic (paroxysmal choreoathetosis/spasticity) antibody
CSE antibody
DYT17 antibody
DYT18 antibody
DYT9 antibody
EIG12 antibody
erythrocyte/brain antibody
Erythrocyte/hepatoma glucose transporter antibody
facilitated glucose transporter member 1 antibody
Glucose transporter 1 antibody
Glucose transporter type 1 antibody
Glucose transporter type 1 erythrocyte/brain antibody GLUT antibody GLUT-1 antibody GLUT1 antibody GLUT1DS antibody GLUTB antibody GT1 antibody GTG1 antibody Gtg3 antibody GTR1_HUMAN antibody HepG2 glucose transporter antibody HTLVR antibody Human T cell leukemia virus (I and II) receptor antibody MGC141895 antibody MGC141896 antibody PED antibody RATGTG1 antibody Receptor for HTLV 1 and HTLV 2 antibody SLC2A1 antibody Solute carrier family 2 (facilitated glucose transporter) member 1 antibody Solute carrier family 2 antibody Solute carrier family 2 facilitated glucose transporter member 1 antibody |
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Molecular Weight(MW) | 54 kDa |
Cellular Localization | Cell membrane, Melanosome |
SwissProt ID | P11166 P17809 P11167 |
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Fig1: Western blot analysis of GLUT1 on different cell lysates using anti-GLUT1 antibody at 1/1000 dilution. Positive control: Lane 1: Hela Lane 2: MCF-7 Lane 3: Jurkat Lane 4: NIH/3T3
Fig2: ICC staining GLUT1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: ICC staining GLUT1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig4: ICC staining GLUT1 in HepG2 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig5: Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig6: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig7: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig8: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig9: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-GLUT1 antibody. Counter stained with hematoxylin.
Fig10: Flow cytometric analysis of Hela cells with GLUT1 antibody at 1/50 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody
Positive Control | Jurkat, MCF-7, Hela, HepG2, NIH/3T3, mouse liver tissue, human liver tissue, human breast carcinoma tissue, human kidney tissue. |
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Application Notes | WB:1:500-1:1,000 ICC:1:50-1:200 IHC:1:50-1:200 FC:1:10-1:100 |
Form | Liquid |
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Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage Buffer | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
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