75 Results for "

FGF2

" in MedChemExpress (MCE) Product Catalog:
Products (75)

75 Results for "FGF2" in MCE Product Catalog:

43
43 Publications Verification
Cat. No.: HY-P7004
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
Species:  
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14
14 Cited Publications
Cat. No.: HY-P7066
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMubFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
Species:  
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9
9 Cited Publications
Cat. No.: HY-P7331
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 154a.a.; bFGF; FGF-2; HBGF-2; FGFB
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5
5 Cited Publications
Cat. No.: HY-P701242
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; Basic fibroblast growth factor; bFGF; Heparin-binding growth factor 2; HBGF-2; FGF2; FGFB
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5
5 Cited Publications
Cat. No.: HY-P7091
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtbFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
Species:  
Rat
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4
4 Cited Publications
Cat. No.: HY-P1408
CAS No.: 404882-00-4
Target:  

Integrin VEGFR

Research Areas:  

Cancer

Obtustatin is a non-RGD disintegrin consisting of 41 residues. Obtustatin inhibits the adhesion of α1β1 integrin to type IV Collagen (HY-NP003), blocks α1β1 integrin signaling in endothelial cells, and suppresses FGF2-induced angiogenesis. Obtustatin inhibits tumor progression in mouse models and upregulates VEGF expression in sarcoma-bearing mice. Obtustatin can be used in research related to Lewis lung carcinoma and S-180 sarcoma [2] .
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4
4 Cited Publications
Cat. No.: HY-P7330
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 145a.a.; bFGF; FGF-2; HBGF-2; FGFB
Species:  
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3
3 Cited Publications
Cat. No.: HY-P73052
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; bFGF; HBGF-2; FGF2
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3
3 Cited Publications
Cat. No.: HY-P7331A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 154a.a.; bFGF; FGF-2; HBGF-2; FGFB
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2
2 Cited Publications
Cat. No.: HY-122704A
CAS No.: 5424-37-3
Synonyms: Aminoquinuride dihydrochloride
Surfen dihydrochloride is a potent heparan sulfate antagonist. Surfen inhibits FGF2 binding and signal transduction. Surfen binds to glycosaminoglycans and reduces tau hyperphosphorylation. Surfen dihydrochloride inhibits the activity of recombinant uronyl 2-O-sulfotransferase with an IC50 of approximately 2 μM. Surfen dihydrochloride inhibits HSV-1 viral infection. Surfen dihydrochloride inhibits neural differentiation, delays remyelination, and alleviates EAE [2] .
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2
2 Cited Publications
Cat. No.: HY-P7179
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rBobFGF; FGF-2; FGF2; FGF 2; HBGF-2
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2
2 Cited Publications
Cat. No.: HY-P700479
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast Growth Factor 2; FGF-2; Basic Fibroblast Growth Factor; bFGF; Heparin-Binding Growth Factor 2; HBGF-2; FGF2; FGF-2
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1
1 Cited Publications
Cat. No.: HY-D0889
CAS No.: 556-50-3
Synonyms: Gly-Gly; H-Gly-Gly-OH
Glycylglycine is a non-selective glycylglycine dipeptidase substrate and iNOS inhibitor. Glycylglycine can cross the cell membrane by passive diffusion and is hydrolyzed to glycine in the cell, participating in energy metabolism and antioxidant processes. Glycylglycine promotes spermatogonial stem cells (SSCs) proliferation, inhibits astrocyte overactivation and reduces nitric oxide (NO) release, while upregulating the expression of neurotrophic factors (such as PDGFA, FGF2, CNTF) to support nerve myelin repair. Glycylglycine can be used to study male reproductive biology (such as SSCs proliferation regulation) and neurodegenerative diseases (such as neuroprotective mechanisms in multiple sclerosis) [2].
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1
1 Cited Publications
Cat. No.: HY-P700237AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; Basic fibroblast growth factor; bFGF; Heparin-binding growth factor 2; HBGF-2; FGF2; FGFB
Species:  
Pig
Source:  
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1
1 Cited Publications
Cat. No.: HY-P70600A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; Basic fibroblast growth factor; bFGF; Heparin-binding growth factor 2; HBGF-2; FGF2; FGFB
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1
1 Cited Publications
Cat. No.: HY-P700630
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast Growth Factor 2; FGF-2; Basic Fibroblast Growth Factor; bFGF; Heparin-Binding Growth Factor 2; HBGF-2; FGF2; FGF-2
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1
1 Cited Publications
Cat. No.: HY-P80671
Synonyms: FGF2; FGFB; Fibroblast growth factor 2; FGF-2; Basic fibroblast growth factor; bFGF; Heparin-binding growth factor 2; HBGF-2

Host:  

Rabbit

Application:  

WB, IP, FC, IHC-P

Reactivity:  

Human, Mouse

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1
1 Cited Publications
Cat. No.: HY-P7330A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 145a.a.; bFGF; FGF-2; HBGF-2; FGFB
Species:  
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Cat. No.: HY-107753
CAS No.: 729605-21-4
Purity:  98.09%
Target:  

Ras

Research Areas:  

Inflammation/Immunology Cancer

XRP44X inhibits Ras-induced transcription activation with the IC50 of 10 nM. XRP44X inhibits activation of the Ras-Erk-1/2 pathway by FGF-2 . XRP44X is an inhibitor of Ras/Erk activation of Elk3 that also affects microtubules [2].
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Cat. No.: HY-107194
CAS No.: 102586-30-1
Purity:  99.07%
NSC12 is an orally active pan-FGF trap. NSC12 inhibits the interaction between FGF2/FGFR. NSC12 suppresses the phosphorylation of FGFR3. NSC12 reduces c-Myc levels, induces DNA damage, triggers the cleavage of Caspase 3, and promotes ROS production. NSC12 exhibits anticancer activity against lung cancer and multiple myeloma [2].
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