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Y00005-002

Chicken IgY anti-Beta-actin antibody

Availability: In stock

$50.00
Immunoaffinity purified Chicken IgY anti-Beta-actin antibody

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Details

Description

Immunoaffinity purified Chicken IgY anti-Beta-actin antibody

Information

Applications No
Additional Info No
Target Protein Beta-actin
Species detected No
Purity Method Immunoaffinity purified
Dilution ICC/IF, 1:100-1:1000; WB, 1:1 000
Storage Store at +4ºC short term (6 months). Aliquot, add 50% glycerol and store at -20ºC. Avoid repeated freeze / thaw cycles.
Research areas No
Isotype IgY
Protocol No
Antibody Category Primary Antibodies

Applications
Additional Info
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
Lysate from expotentially-growing Jurkat cells. 10 µg per well of sample was run on 12 % gel and transferred to nitrocellulose membrane. Blocking was performed using 3% non-fat milk in PBST for 1 h at room temperature. Anti-Beta actin primary antibody (Y0
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