Vascular endothelial growth factor A

Vascular endothelial growth factor A

Member of the PDGF/VEGF growth factor family

Horse Serum Formulation

Human Endothelial Growth Medium-Serum Free Formulation 1 (EGM-SF1)

cAP-02-SF1 500ml
EUR 133.65

Horse Serum Laboratories manufactures the horse serum formulation reagents distributed by Genprice. The Horse Serum Formulation reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Horse Serum. Other Horse products are available in stock. Specificity: Horse Category: Serum Group: Formulation

Serum albumin

1mg
EUR 2640

Serum albumin

1mg
EUR 2640

Serum albumin

1mg
EUR 2640

Serum albumin

1mg
EUR 2640

Goat serum

10 nmol
EUR 287.5

Goat serum

5 nmol
EUR 237.5

Alpaca Serum

10 nmol
EUR 1462.5

Formulation information

Lificiguat (YC-1) Liposomes, Formulation FNT8P.2

DLL-0016-A1-10ML 10mL
EUR 2995
Description: PEGylated liposomes containing HIF-1α inhibitor Lificiguat (YC-1). Lificiguat (YC-1) is an inhibitor of Hypoxia-inducible factor-1 alpha (HIF-1 alpha). YC-1 also activates soluble guanylyl cyclase (sGC) in (NO)-independent manner. Lificiguat (YC-1) is insoluble in aqueous media. This product is a pre-formulated liposomal version of Lificiguat which is supplied ready to use in vitro or in vivo. The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1A-100MG 10 mL
EUR 2995
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1A-10MG 1 mL
EUR 595
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1A-25MG 2.5 mL
EUR 995
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1B-100MG 10 mL
EUR 3195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1B-10MG 1 mL
EUR 795
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1B-25MG 2.5 mL
EUR 1195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1C-100MG 10 mL
EUR 3195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1C-10MG 1 mL
EUR 795
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1C-25MG 2.5 mL
EUR 1195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1D-100MG 10 mL
EUR 3195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1D-10MG 1 mL
EUR 795
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1D-25MG 2.5 mL
EUR 1195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1E-10MG 1 mL
EUR 795
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1E-25MG 2.5 mL
EUR 1195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Mirdametinib (PD0325901) Liposomes, Formulation U6-2

DLL-0008-1E-50MG 5 mL
EUR 3195
Description: PEGylated liposomes containing MEK inhibitor Mirdametinib (PD0325901). Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with an IC50 of 0.33 nM (cell-free assays). The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.

Alternate BTEX Standard Formulation (High Level) - 1ML

BTEX-100H 1ML
EUR 56.7