Gontijo Et Al.

Endothelin-1 (ET-1), big (Human) - Purified IgG Antibody

G-023-10 400 μg
EUR 438.48

Human IgG antibody Laboratories manufactures the gontijo et al. reagents distributed by Genprice. The Gontijo Et Al. 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 . Other Gontijo products are available in stock. Specificity: Gontijo Category: Et Group: Al.

True Blue

5mg Ask for price
Description: True Blue

al Antibody

0.2mg Ask for price
Description: Recombinant Drosophila melanogaster (Fruit fly) al protein

al Antibody

10mg Ask for price
Description: Recombinant Drosophila melanogaster (Fruit fly) al protein

Endothelin-1 (ET-1), big (22-38) (Human) - Purified IgG Antibody

400 μg
EUR 438.48

prepro-Endothelin-1 (ET-1) (18-50) (Human) - Purified IgG Antibody

400 μg
EUR 438.48

Human True Insulin ELISA Kit

10x96-Strip-Wells
EUR 6725

Human True Insulin ELISA Kit

48-Strip-Wells
EUR 550

Al. information

AL 8810

B4575-25 25 mg
EUR 2172.8
Description: GPCR/G protein|Prostaglandin Receptor

AL 8810

B4575-5 5 mg
EUR 559.2
Description: GPCR/G protein|Prostaglandin Receptor

AL 8697

B7784-10 10 mg
EUR 556.8
Description: AL8697 is a selective p38 MAPK(mitogen-activated protein Kinase) inhibitor, which is also named P38 ? inhibitor. It has the function of inhibiting the activity of P38 MAPK.

AL 8697

B7784-5 5mg
EUR 516
Description: MAPK Signaling|p38

AL 8697

B7784-50 50 mg
EUR 2154
Description: AL8697 is a selective p38 MAPK(mitogen-activated protein Kinase) inhibitor, which is also named P38 ? inhibitor. It has the function of inhibiting the activity of P38 MAPK.

al Antibody

CSB-PA312366XA01DLU-02mg 0.2mg Ask for price
Description: Recombinant Drosophila melanogaster (Fruit fly) al protein

al Antibody

CSB-PA312366XA01DLU-10mg 10mg Ask for price
Description: Recombinant Drosophila melanogaster (Fruit fly) al protein

AL 34662

C5271-10 10 mg
EUR 107.2
Description: Neuroscience|5-HT Receptor

AL 34662

C5271-50 50 mg
EUR 465.6
Description: Neuroscience|5-HT Receptor

AL-438

HY-114154 Get quote Ask for price
Description: AL-438 is a potent, selective and orally active glucocorticoid receptor modulator with Kis of 2.5, 1786, 53, 1440, >1000 nM for glucocorticoid receptor, progesterone receptor, mineralocorticoid receptor, androgen receptor, estrogen receptor, respectively. AL-438 shows antiinflammatory activity[1][2].

AL-8810

HY-100449 1 mg
EUR 238.1
Description: AL-8810 is a potent and selective antagonist of the PGF 2α receptor (FP receptor). AL-8810 is an activator of MAPK and ERK1/2. The Ki of the FP receptor of mouse 3T3 cells and rat A7r5 cells are 0.2±0.06 μM and 0.4±0.1 μM, respectively. AL-8810 can be used in the study of elevated intraocular pressure (OHT) and primary open-angle glaucoma (POAG)[1][2][3][4][5].

AL 8697

HY-108645 5mg
EUR 378.79
Description: AL 8697 is a specific and orally active p38α MAPK inhibitor with an IC50 of 6 nM. AL 8697 displays 14-fold greater inhibition of p38α compared to p38β (IC50=82 nM), and 300-fold selectivity for p38α over a panel of 91 kinases. Anti-inflammatory activity[1].

AL 082D06

HY-15709 100mg
EUR 392.86
Description: AL 082D06 is a selective, nonsteroidal glucocorticoid receptor (GR) antagonist with Ki of 210 nM.

AL-34662

HY-125641 5mg
EUR 132.04
Description: AL-34662 is a selective 5-HT2A receptoragonist (IC50: 0.77 nM and 1.5 nM for rat and human 5-HT2 receptor). AL-34662 is also a weak α-1D adrenergic agonist activity (EC50:0.4 μM). AL-34662 is an ocular hypotensive agent[1][2].

Al-901

E40YR1103 1 mg
EUR 2960
Description: Available in various conjugation types.

AL-8417

HY-117368 Get quote Ask for price
Description: AL-8417 ((2R)-AL-5898) is a potent inhibitor of Cyclooxygenase (COX), with IC50 of 120 μM, that plays an important role in inflammatory response[1].

AL-9

HY-118525 Get quote Ask for price
Description: AL-9 is a inhibitor of PI4KIIIα, with the IC50 of 0.57 μM, that can inhibit HCV replication[1].