Antibodies

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DF4526 staining MCF7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC24A6 Antibody
From $537.37
DF4525 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC24A4 Antibody
From $537.37
Western blot analysis of extracts from Hela, using SLC24A3 Antibody. Lane 1 was treated with the blocking peptide.
Affinity Biosciences SLC24A3 Antibody
From $537.37
Western blot analysis of extracts from Hela, using SLC24A1 Antibody. Lane 1 was treated with the blocking peptide.
Affinity Biosciences SLC24A1 Antibody
From $537.37
DF4522 staining Hela by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. Samples were then incubated with primary Ab(DF4522 1:200) and mouse anti-beta tubulin Ab(T0023 1:200) for 1 hour at 37¡ãC. An AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(S0006 Red 1:600) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(S0017 Green 1:600) were used as the secondary antibod
Affinity Biosciences SLC28A2 Antibody
From $537.37
Western blot analysis of extracts from 293, using SLC5A3 Antibody. Lane 1 was treated with the blocking peptide.
Affinity Biosciences SLC5A3 Antibody
From $537.37
Western blot analysis of extracts from various samples, using SLC9A9 Antibody. Lane 1: 293 treated with blocking peptide. Lane 2: 293; Lane 3: Hela;
Affinity Biosciences SLC9A9 Antibody
From $537.37
DF4519 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC9A8 Antibody
From $537.37
Western blot analysis of extracts from Hela and mouse lung, using SLC9A7 Antibody.
Affinity Biosciences SLC9A7 Antibody
From $537.37
DF4517 staining RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod
Affinity Biosciences SLC9A6 Antibody
From $537.37
DF4516 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC5A2 Antibody
From $537.37
Western blot analysis of extracts from mouse liver cells, using SLC10A7 antibody.
Affinity Biosciences SLC10A7 Antibody
From $537.37
DF4514 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SCN2B Antibody
From $537.37
DF4513 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SCN4A Antibody
From $537.37
DF4512 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SCN4B Antibody
From $537.37
Western blot analysis of extracts from mouse brain, using SLC4A11 Antibody. Lane 1 was treated with the blocking peptide.
Affinity Biosciences SLC4A11 Antibody
From $537.37
DF4510 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC6A1 Antibody
From $537.37
DF4509 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SLC6A8 Antibody
From $537.37
DF4508 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SIRPG Antibody
From $537.37
DF4507 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Affinity Biosciences SIRPB1 Antibody
From $537.37
DF4506 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod
Affinity Biosciences SHC2 Antibody
From $537.37
DF4505 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod
Affinity Biosciences SH3GL2 Antibody
From $537.37
Western blot analysis of extracts from Mouse muscle, using SH3RF3 Antibody. The lane on the left was treated with blocking peptide.
Affinity Biosciences SH3RF3 Antibody
From $537.37
DF4503 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Affinity Biosciences SH3GLB2 Antibody
From $537.37

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