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The protein encoded by IKBKAP is a scaffold protein and a regulator for 3 different kinases involved in proinflammatory signaling. Additionally we are shipping Inhibitor of kappa Light Polypeptide Gene Enhancer in B-Cells, Kinase Complex-Associated Protein Proteins (4) and many more products for this protein.
Showing 10 out of 85 products:
Human Monoclonal IKBKAP Primary Antibody for WB - ABIN393871
Bailey, Xie, Do, Montpetit, Diaz, Mohan, Keavney, Yusuf, Gerstein, Engert, Anand: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. in Diabetes Care 2010
Show all 5 references for ABIN393871
Human Polyclonal IKBKAP Primary Antibody for EIA, IF - ABIN499964
Anderson, Coli, Daly, Kichula, Rork, Volpi, Ekstein, Rubin: Familial dysautonomia is caused by mutations of the IKAP gene. in American journal of human genetics 2001
Show all 4 references for ABIN499964
Human Monoclonal IKBKAP Primary Antibody for IHC (p), ELISA - ABIN563666
Lefler, Cohen, Kantor, Cheishvili, Even, Birger, Turetsky, Gil, Even-Ram, Aizenman, Bashir, Maayan, Razin, Reubinoff, Weil: Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation. in PLoS ONE 2015
show that the Elongator (elo1, elo2, and elo3) complex was purified from plant cell cultures as a six-component complex.
Elongator is important for plants to respond to ABA and drought exposure and that ABO1/ELO2 may play a vital role in ABA signal transduction pathways.[ABO1]
ELP1 has a neuron autonomous role in sympathetic and sensory target tissue innervation
Phosphatidylserine increases IKBKAP levels in a humanized knock-in IKBKAP mouse model for Familial dysautonomia.
Familial dysautonomia model reveals Ikbkap deletion causes apoptosis of Pax3 (show PAX3 Antibodies)+ progenitors and peripheral neurons.
our study not only reveals a novel function of IKAP in meiosis, but also suggests that IKAP contributes to this process partly by exerting its effect on transcription and tRNA modification
IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia.
IKAP is essential for expression of specific genes involved in cardiac morphogenesis (show XIRP1 Antibodies), and cardiac failure is the likely cause of abnormal vascular development and embryonic lethality; deletion of exon 20 abolishes gene function
mutations in the human I-kappaB kinase-associated protein (IKBKAP) gene are responsible for familial dysautonomia (FD).no animal model of FD currently exists, cloning of the mouse Ikbkap gene is an important step toward creating a mouse model for FD
description of a humanized IKBKAP transgenic mouse that models a tissue-specific human splicing defect
IKAP is crucial for both vascular and neural development during embryogenesis and that protein function is conserved between mouse and human.
IKAP might be a vesicular like protein that might be involved in neuronal transport in hESC derived PNS neurons
The formation of the Elp1 dimer contributes to its stability in vitro and in vivo and is required for the assembly of human Elongator complexes.
IKBKAP mRNA levels decreased during a familial dysautonomia crisis and returned to baseline after recovery. The cause-and-effect relationship is unclear.
Digoxin-mediated repression of SRSF3 (show SRSF3 Antibodies) expression plays a role in the digoxin-mediated inclusion of exon 20 in the IKBKAP transcript generated from the familial dysautonomia mutant allele.
Combined treatment with epigallocatechin gallate and genistein synergistically upregulates wild-type IKBKAP-encoded RNA and protein levels in familial dysautonomia-derived cells.
IKAP plays pleiotropic roles in both the peripheral and central nervous systems
IKAP/hELP1 deficiency has an effect on gene expression in differentiating neuroblastoma (show ARHGEF16 Antibodies) cells, and possibly on familial dysautonomia
IKK complex-associated protein deficiency upregulates the microtubule destabilizing protein SCG10 (show STMN2 Antibodies) and, in parallel, disorganizes the cytoskeleton
Phosphatidylserine increases IKBKAP levels in familial dysautonomia cells
The protein encoded by this gene is a scaffold protein and a regulator for 3 different kinases involved in proinflammatory signaling. This encoded protein can bind NF-kappa-B-inducing kinase (NIK) and IKKs through separate domains and assemble them into an active kinase complex. Mutations in this gene have been associated with familial dysautonomia.
elongator complex protein 1
, inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
, IKK complex-associated protein
, IKK-complex-associated protein IKAP
, ikappaB kinase complex-associated protein
, inhibitor of kappa light polypeptide enhancer in B-cells, kinase complex-associated protein
, elongator acetyltransferase complex subunit 1
, putative elongator complex protein 1