WB
The effects of genetic abnormality-induced cytological and spectral alterations in AML cells. (a) Ratio of clone formation. (b) Relative contents of Raman bands screened by CRT algorithm. (c) Western blot analysis showed the c-KIT and p-c-KIT expression, GAPDH served as loading control, along with (d) ratio of phosphorylated c-KIT to total c-KIT. *P<0.05.
IHC
Phospho-c-Kit (Tyr721) Antibody at 1/200 staining Rat ganstric tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue was then blocked and incubated with the antibody for 1.5 hours at 22°C. An HRP conjugated goat anti-rabbit antibody was used as the secondary antibody.
IHC
Phospho-c-Kit (Tyr721) Antibody at 1/200 staining Human heart tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue was then blocked and incubated with the antibody for 1.5 hours at 22°C. An HRP conjugated goat anti-rabbit antibody was used as the secondary antibody.
IHC
Phospho-c-Kit (Tyr721) Antibody at 1/200 staining Mouse kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue was then blocked and incubated with the antibody for 1.5 hours at 22°C. An HRP conjugated goat anti-rabbit antibody was used as the secondary antibody.