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Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Zusätzlich bieten wir Ihnen CLPB Proteine (4) und CLPB Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal CLPB Primary Antibody für ELISA - ABIN314275
Satpute-Krishnan, Langseth, Serio: Hsp104-dependent remodeling of prion complexes mediates protein-only inheritance. in PLoS biology 2007
Case Reports: bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel disorder of mitochondrial protein (zeige COX6B2 Antikörper) disaggregation.
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria
ClpB can passively thread soluble denatured proteins.
Mutations in CLPB define a syndrome with intellectual disability, congenital neutropenia, progressive brain atrophy, movement disorder, cataracts, and 3-methylglutaconic aciduria.
CLPB is proposed to function as a mitochondrial chaperone involved in disaggregation of misfolded proteins, resulting from stress such as heat denaturation.
ClpB-DnaK reactivated all aggregated fusion proteins with similar efficiency, without unfolding native domains, demonstrating that partial threading of the misfolded moiety is sufficient to solubilize aggregates.
formation of the DnaK-ClpB bichaperone network is a three step process
Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene is a receptor for ephrin-B family members.
caseinolytic peptidase B protein homolog
, suppressor of potassium transport defect 3
, ClpB caseinolytic peptidase B homolog
, suppressor of K+ transport defect 3