Apexbio Technology

Lab Reagents

Apexbio Reagents Laboratories manufactures the apexbio technology reagents distributed by Genprice. The Apexbio Technology 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 Apexbio Reagents. Other Apexbio products are available in stock. Specificity: Apexbio Category: Technology

Human Samples information

LH 21

C3642-5 5 mg
EUR 345
Description: IC50: 631 ±98 and 690 ± 41 nM for human and rat CB1 receptors, respectivelyLH 21 is a CB1 antagonist. The endogenous cannabinoid system plays a critical modulatory role in feeding behavior and metabolism, acting at both peripheral and central levels.

Danazol

C3644-100 100 mg
EUR 110
Description: Danazol showed weak androgenic effects.Danazol is a derivative of testosterone and ethisterone. An androgen is any natural or synthetic agent stimulating or controling the development and maintenance of male characteristics by binding to androgen receptors.

Danazol

C3644-250 250 mg
EUR 187
Description: Danazol showed weak androgenic effects.Danazol is a derivative of testosterone and ethisterone. An androgen is any natural or synthetic agent stimulating or controling the development and maintenance of male characteristics by binding to androgen receptors.

Danazol

C3644-500 500 mg
EUR 312
Description: Danazol showed weak androgenic effects.Danazol is a derivative of testosterone and ethisterone. An androgen is any natural or synthetic agent stimulating or controling the development and maintenance of male characteristics by binding to androgen receptors.

ML-211

C3647-1 1 mg
EUR 112
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

ML-211

C3647-10 10 mg
EUR 270
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

ML-211

C3647-25 25 mg
EUR 519
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

ML-211

C3647-5 5 mg
EUR 174
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

Stachydrine (hydrochloride)

C3648-100 100 mg
EUR 119
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-1000 1 g
EUR 467
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-250 250 mg
EUR 206
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-500 500 mg
EUR 328
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Ceranib-2

C3649-10 10 mg
EUR 179
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-25 25 mg
EUR 357
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-5 5 mg
EUR 118
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-50 50 mg
EUR 595
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

ALK5 Inhibitor II (hydrochloride)

C3656-10 10 mg
EUR 176
Description: IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-? cellular assay, and ALK5 binding in HepG2 cells, respectivelyALK5 Inhibitor II is an ALK5 inhibitor.The TGF-beta family of cytokines signal via serine/threonine kinase transmembrane type I and type II receptors.