The largest database of trusted experimental protocols

Igf2bp2

Manufactured by Santa Cruz Biotechnology
Sourced in United States

IGF2BP2 is a protein that binds to insulin-like growth factor 2 mRNA and plays a role in its localization, stability, and translation. It is involved in various cellular processes, including cell growth, differentiation, and development.

Automatically generated - may contain errors

3 protocols using igf2bp2

1

Immunohistochemical Profiling of Cancer Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
The de-paraffinized sections were incubated with 20% goat serum for 30 min and were incubated with primary antibodies against Ct-OATP1B3 (1:200, Abcam, USA), IGF2BP2 (1:100, Santa Cruz, USA), CPT1A (1:1000, Abcam, USA), and NDUFA2 (1:100, Abcam, USA) at 4 °C overnight followed by the secondary antibody for 1 h at 37 °C. The calculation method of IHC score was performed as described previously [49 (link)]. Ct-OATP1B3 expression level was analyzed by classifying IHC score as low (based on the IHC score lower than the median value) and as high (based on an IHC score higher than the median value).
+ Open protocol
+ Expand
2

Silencing Alkbh5 and Igf2bp2 in Cells and Oocytes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Small interference RNA (siRNA) of murine Alkbh5 and Igf2bp2 were purchased from Santa Cruz (sc-141022) and GenePharma respectively. For gene knockdown in cell lines, mGC was transfected with siRNA via Lipofectamine™ RNAiMAX (Invitrogen, 13778150). Protein analysis was performed 48 h after transfection. For RNA interference in oocytes, approximately 5–10 pl siRNA diluted with RNase-free water (60 μM) was microinjected into GV oocytes as detailed in the followings.
+ Open protocol
+ Expand
3

Comprehensive Immunoblotting Analysis of Muscle Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total protein of the cell or tissue samples was harvested using radioimmunoprecipitation lysis buffer after washing three times with PBS. Immunoblotting was carried out according to our previous method (10 (link)). The primary antibodies targeted the following proteins: MyHC (1:500; no. MAB4470; R and D Systems), MyoD (1:500; no. NB100-56511; Novus Biologicals), AKT (1:1000; no. 9272S; CST), p-AKT (Ser473) (1:2000; no. 4060S; CST), PI3K (p55α) (1:1000; no. 11889S; CST), p-PI3K p55 (Tyr199) (1:1000; no. 4228S; CST), β-tubulin (1:200; no. sc-58880; Santa Cruz Biotechnology), MyoG (1:1000; no. NB100-56510SS; Novus Biologicals), MuRF1 (1:200; no. sc-398608; Santa Cruz Biotechnology), MAFbx (1:200; no. sc-166806, Santa Cruz Biotechnology), cyclin E (1:100; no.sc-377100; Santa Cruz Biotechnology), cyclin D1 (1:100; no. sc-450; Santa Cruz Biotechnology), PTEN (1:500; no. sc-7974; Santa Cruz Biotechnology), IGF2BP2 (1:100; no. sc-377014; Santa Cruz Biotechnology), and proliferating cell nuclear antigen (1:100; no. sc-56; Santa Cruz Biotechnology). The secondary antibodies included goat anti-rabbit IgG (1:3000; no. BA1054; BosterBio) and goat antimouse IgG (1:3000; no. BA1050; BosterBio).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!