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The protein encoded by ABCC9 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Additionally we are shipping ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 9 Kits (9) and ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 9 Proteins (8) and many more products for this protein.
Showing 10 out of 75 products:
Chicken Polyclonal ABCC9 Primary Antibody for WB - ABIN2781513
Burke, Mutharasan, Ardehali: The sulfonylurea receptor, an atypical ATP-binding cassette protein, and its regulation of the KATP channel. in Circulation research 2008
single amino acid difference can account for the markedly different diazoxide sensitivities between channels containing either the SUR1 (show ABCC8 Antibodies) or SUR2A subunit isoforms.
We describe novel ABCC9 variants in human brain, corresponding to altered 3'UTR (show UTS2R Antibodies) length, which could lead to targeting by miR (show MLXIP Antibodies)-30c
Results show that a polymorphism in ABCC9 is associated with aging pathology, and exposure to sulfonylurea drugs is associated with increased risk for aging pathology among individuals who died age 85 and older
This study confirmed that specific ABCC9 single-nucleotide polymorphisms is associated with HS-Aging pathology in the Alzheimer disease.
ABCC9 is a susceptibility gene for early repolarization syndrome and Brugada syndrome.
A mutation (V734I) in ABCC9 increases susceptibility to coronary spasm and acute myocardial infarction.
This study showed that variants in the SUR2 (show MED23 Antibodies) gene (ABCC9) associate with epidemiological variation in human sleep duration, which is also influenced by inter-individual differences in seasonal adaptation and chronotype.
Electrophysiological experiments show that mutations in ABCC9, associated with Cantu syndrome, reduce the ATP-mediated potassium channel (show KCNAB2 Antibodies) inhibition, resulting in channel opening.
Cantu syndrome is caused by mutations in ABCC9
mammalian oocytes express K(ATP) channels. Real-time PCR revealed that mRNA for Kir6.1 (show KCNJ8 Antibodies), Kir6.2 (show KCNJ11 Antibodies), SUR2A and SUR2B, were present in human oocytes of different stages.
Results describe a new function of the Kir6.1 (show KCNJ8 Antibodies)-SUR2A complex, namely the regulation of paracellular permeability through tight junctions.
Kir6.1/SUR2B is the major functional K(ATP) channel complex in the pig MMA and MCA, and mRNA expression studies suggest that the human MMA shares this K(ATP) channel subunit profile
Data show that PI3K/Akt (show AKT1 Antibodies) signalling pathway and lactate dehydrogenase (LDH) play a crucial role in increase of cardiac ATP-binding cassette transporter sub-family C member 9 (SUR2A) induced by in vivo exposure to 18% oxygen.
Sulfhydration of SUR2B subunit modifies tyrosine nitration of Kir6.1 (show KCNJ8 Antibodies) subunit within the KATP channel complex.
ATP-sensitive potassium currents from channels formed by Kir6 and a modified cardiac mitochondrial SUR2 variant
In the absence of Abcc9, the newborn heart fails to transition normally from fetal to mature myocardial metabolism.
Native K(ATP) channels in mouse vas (show AVP Antibodies) deferens myocytes are a heterocomplex of K(IR)6.1 channels and SUR2B subunits.
The results confirm that Kir6.2 (show KCNJ11 Antibodies) contributes to APD shortening in both atria and ventricle during metabolic stress, and that SUR1 (show ABCC8 Antibodies) is required for atrial APD shortening while SUR2A is required for ventricular APD shortening.
the role of CpG methylation in regulating SUR1 (show ABCC8 Antibodies) and SUR2 expression
Report unique properties of the ATP-sensitive potassium channel (show KCNAB2 Antibodies) in the mouse ventricular cardiac conduction system.
Syntaxin-1A (show STX1A Antibodies) inhibits KATP channels by interacting with specific conserved motifs within sulfonylurea receptor (show ABCC8 Antibodies) 2A.
Results suggest that oral nicotinamide is a regulator of SUR2A expression and has a potential as a drug that can improve physical endurance in conditions where this effect would be desirable.
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is thought to form ATP-sensitive potassium channels in cardiac, skeletal, and vascular and non-vascular smooth muscle. Protein structure suggests a role as the drug-binding channel-modulating subunit of the extra-pancreatic ATP-sensitive potassium channels. Mutations in this gene are associated with cardiomyopathy dilated type 1O. Alternative splicing results in multiple transcript variants.
ATP-binding cassette, sub-family C, member 9
, ATP-binding cassette, sub-family C (CFTR/MRP), member 9
, ATP-binding cassette sub-family C member 9
, ATP-binding cassette sub-family C member 9-like
, sulfonylurea receptor subunit 2
, ATP-binding cassette transporter sub-family C member 9
, sulfonylurea receptor 2
, sulfonylurea-binding protein 2
, Sulfonylurea receptor 2
, cardiac ventricle sulfonyl urea receptor
, sulphonylurea receptor 2B