FGF basic/FGF2 Antibody

Name	FGF basic/FGF2 Antibody
Supplier	Novus Biologicals
Catalog	NB600-1536
Prices	$279.00
Sizes	100 µl
Host	Rabbit
Clonality	Polyclonal
Applications	WB ELISA IHC IHC-P
Species Reactivities	Human, Rat, Bovine, Horse
Antigen	Synthetic peptide conjugated to KLH, corresponding to amino acids 1-24 of Cow FGF2.
Purity/Format	Sterile filtered
Description	Rabbit Polyclonal
Gene	FGF2
Conjugate	Unconjugated
Supplier Page	Shop

Product images

Immunohistochemistry: FGF basic/FGF2 Antibody [NB600-1536] - Immunoperoxidase staining (PAP) of U87MG glioma cell suspension implanted into nude rat brain (Han rnu/rnu) using Rabbit Anti-Fibroblast Growth Factor-Basic (NB600-1536). High bFGF expression is exclusively shown within tumor endothelial cells. The tissue sample was paraffin-embedded and 4% Tris-buffered formalin-fixed without any enzymatic or antigen-demasking pre-processing. From Dr. A.-C. Stan, Institute of Neuropathology, Medical School Hannover, Hannover, Germany. Ref: Stan, A.C., et al., J. Neurosurg., 82, 1044 (1995).

Immunohistochemistry: FGF basic/FGF2 Antibody [NB600-1536] - Immunoperoxidase staining (PAP) of a fibrillary differentiated astrocytoma (WHO grade I, SAMS grade 1) using Rabbit Anti-Fibroblast Growth Factor-Basic. High bFGF expression is shown within tumor cells as well as within endothelial cells.

Immunohistochemistry: FGF basic/FGF2 Antibody [NB600-1536] - Immunoperoxidase staining (PAP) of a gemistocytic differentiated area of an anaplastic astrocytoma (WHO grade III, SAMS grade 3) using Rabbit Anti-Fibroblast Growth Factor-Basic. High bFGF expression is shown within tumor cells as well as within the endothelial cells.

Immunohistochemistry: FGF basic/FGF2 Antibody [NB600-1536] - Immunoperoxidase staining (PAP) of a freshly explanted gliobastoma multiforme (WHO grade IV, SAMS grade 4) in culture (passage # 3) using Rabbit Anti-Fibroblast Growth Factor-Basic (NB600-1356). Intracytoplasmatically, homogeneous, high bFGF expression is shown within highly polymorphic tumor cells. The tumor cells on glass coverslips were methanol/acetone (100%, ice-cold, 1:1) fixed without any enzymatic or antigen-demasking pre-processing. From Dr. A.-C. Stan, Institute of Neuropathology, Medical School Hannover, Hannover, Germany.