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Goat anti rabbit immunoglobulin ig g h l

Manufactured by Proteintech
Sourced in United States

Goat Anti-Rabbit immunoglobulin (Ig) G (H+L) is a secondary antibody used in immunoassays and other applications that require detection of rabbit primary antibodies. This antibody is produced by immunizing goats with rabbit IgG and recognizes both the heavy (H) and light (L) chains of rabbit immunoglobulin.

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2 protocols using goat anti rabbit immunoglobulin ig g h l

1

Western Blot Analysis of Liver Tissue Proteins

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Total protein was extracted from liver tissue, using RIPA protein lysis buffer containing 1 mM PMSF. 300 ng total protein were separated by 10% SDS-PAGE gel at 80 V for 1 h, transfered with polyvinylidenedifluoride (PVDF) membrane at 100 V for 1.5 h, blocked in 5% BSA (Solarbio, Beijing, China) and probed with appropriate primary antibodies against the target proteins. PTEN (Cat:#9188S), PI3 Kinase p85 (Cat:#4292S) anti bodies were purchased from Cell Signaling (Beverly, MA, USA). p-Akt (Cat:66444-1-Ig) and β-actin (Cat:20536-1-AP) anti bodies were purchased from Proteintech (Protein tech, Chicago, IL, USA). These were followed by incubation with Goat Anti-Rabbit immunoglobulin (Ig) G (H+L) (Cat:SA00001-2) (Protein tech, Chicago, IL, USA), and antigen-antibody complexes were visualized using the chemilucent ECL (TransGen Biotech, Beijing, China) detection system. The densitometric analysis conducted by Image J software 1.6.0 (National Institutes of Health, Bethesda, MD, USA) [37 (link),38 (link),39 (link)].
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2

Investigating PTEN/PI3K/Akt Signaling in Hepatoma Cells

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The human hepatoma cell line SMMC-7721 was plated in 6-well plates at a density of 5 × 104 per well. After overnight culture, the TF at concentration of 1.0 mg/mL was added to the wells and cells were incubated for 48 h. Protein extracts were isolated from each group cells in using RIPA protein lysis buffer containing 1 mM PMSF. Total protein was separated by 10% SDS-PAGE, transferred with polyvinylidenedifluoride (PVDF) membrane, blocked in 5% BSA (Solarbio, Beijing, China), and probed with appropriate primary antibodies against the target proteins. PTEN, PI3 Kinase p85, p-Akt, andβ-actin antibodies were purchased from Cell Signaling (Beverly, MA, USA). These were followed by incubation with Goat Anti-Rabbit immunoglobulin (Ig) G (H + L) (Protein tech, USA), and antigen-antibody complexes were visualized using the chemilucent ECL (TransGen Biotech, China) detection system. The densitometric analysis was conducted by using custom Image J-based software, as reported earlier [19 (link), 20 (link)].
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