Biochemicals and Reagents

JNJ 42041935 is a pharmacologic agent that inhibits the growth of cancer cells and may be used to treat chronic kidney disease. This drug binds to the extracellular matrix, which prevents the proliferation of cells in the tissue. JNJ 42041935 has been shown to inhibit the production of messenger RNA in urine samples taken from patients with chronic kidney disease. The clinical studies have shown that JNJ 42041935 can reduce the incidence of leukemia and blood disorders. The effective dose for this drug is not yet known, but it is thought that it may be around 1-10 mg/kg daily. It is also unknown how long JNJ 42041935 will remain in the body or what its excretion rate is.

Mouse monoclonal KIAA0495 antibody

Rabbit polyclonal STAM2 antibody

Please enquire for more information about Des-methylformate eplerenone including the price, delivery time and more detailed product information at the technical inquiry form on this page

WEHI-345 analog is a peptide that can be used as a research tool. It can be used to study protein interactions, antibody binding, cell biology, ligand binding, pharmacology, and life science. WEHI-345 analog has been shown to inhibit receptors and ion channels. The CAS number for this compound is 1354825-62-9. This compound is of high purity and has been shown to activate some ion channels.

PI3Kα and PI3Kδ inhibitor

The SSRP1 antibody is a highly potent growth factor that acts as a phosphatase in various bioassays. It is specifically activated by human serum and has neutralizing properties. This antibody, widely used in Life Sciences research, targets tyrosine kinase receptors and 3-kinases to regulate cellular processes. It can be utilized in electrode-based experiments and is commonly employed in the field of Antibodies research. Additionally, the SSRP1 antibody has been found to exhibit genotoxic effects and shows potential as an anti-beta amyloid agent for combating amyloid protein-related disorders.

4-[2-(Cyclopropylmethoxy)-5-(methylsulfonyl)phenyl]-2-methyl-1(2H)-isoquinolinone is a small molecule that binds to the leucine-binding site of the NMDA receptor and blocks the channel. This inhibition causes an increase in extracellular glutamate, which inhibits neuronal activity. 4-[2-(Cyclopropylmethoxy)-5-(methylsulfonyl)phenyl]-2-methyl-1(2H)-isoquinolinone is used as a research tool to study ion channels and their interactions with other proteins. It has been shown to bind to peptides in high purity, and can be used for antibody production.

Please enquire for more information about 2-Amino-7-(hydroxymethyl)-4(3H)-pteridinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Phm-27 (human) is a peptide that is an activator of the human protein C receptor. It has been shown to inhibit the activity of ion channels and increase cell permeability, as well as act as an anti-inflammatory agent. Phm-27 binds to three different types of receptors: GPCRs, immunoglobulin superfamily proteins, and protease receptors. This peptide also inhibits the binding between two ligands, such as a hormone and its receptor.

NSC305787 is a small molecule modulator, which is derived from synthetic sources. It exhibits its mode of action by interfering with specific cell signaling pathways, ultimately influencing cellular processes. The compound is particularly known for its ability to inhibit or modify the activity of certain proteins involved in these pathways, offering insight into cellular behavior and potential intervention points for various biological systems.