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Dog (Canine) Monoclonal SPTB Primary Antibody für FACS, ICC - ABIN152731
Martin, Golden, Okerblom, Camboni, Chandrasekharan, Xu, Varki, Flanigan, Kornegay: A comparative study of N-glycolylneuraminic acid (Neu5Gc) and cytotoxic T cell (CT) carbohydrate expression in normal and dystrophin-deficient dog and human skeletal muscle. in PLoS ONE 2014
Monoclonal SPTB Primary Antibody für IF, IP - ABIN534235
Tani, Ylänne, Virtanen: Expression of megakaryocytic and erythroid properties in human leukemic cells. in Experimental hematology 1996
Show all 2 Pubmed References
Human Polyclonal SPTB Primary Antibody für IHC, IHC (p) - ABIN4355576
Huang, Zhang, Ho, Oses-Prieto, Burlingame, Lalonde, Noebels, Leterrier, Rasband: αII Spectrin Forms a Periodic Cytoskeleton at the Axon Initial Segment and Is Required for Nervous System Function. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2017
Results of this study provide evidence for a role for spectrin in different steps of megakaryocyte development through its participation in the formation of invaginated membranes and in the maintenance of proplatelet structure.
Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China.
two sex-specific loci(SPTB in females and IZUMO3 in males), yielding associations that were particularly strong at a specific skeletal site, were identified.
Using Next-Generation sequencing, we identified the causative genetic mutations in fifteen patients with clinically suspected hereditary elliptocytosis and hereditary pyropoikilocytosis and correlated the identified mutations with the clinical phenotype and ektacytometry profile.
Targeted next generation sequencing identifies a novel beta-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
Mutational characteristics of ANK1 and SPTB genes in Korean hereditary spherocytosis have been described.
a new mutation in the SPTB gene (466insG) leading to a frameshift and a premature stop codon 29 codons downstream in the region encoding the C-terminal part of the dimerization domain; instability of mutant mRNA results in spectrin deficiency and clinically moderate to serious hereditary spherocytosis
Variations in both alpha-spectrin (SPTA1) and beta-spectrin ( SPTB ) were found in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.
analysis of glycosylation of erythrocyte spectrin and its modification in visceral leishmaniasis
A protein encoded by this locus was found to be differentially expressed in postmortem brains from patients with atypical frontotemporal lobar degeneration.
Data postulate that direct interactions between spectrin ankBDn and PE-rich domains play an important role in stabilizing the structure of the spectrin-based membrane skeleton.
Results suggest that it is possible for cellular proteins to differentially associate with the C-termini of different beta-spectrin isoforms to regulate alpha- and beta-spectrin association to form functional spectrin tetramers.
through the use of an ATP-driven phospholipid translocase (flippase), erythrocytes have evolved a protective mechanism against spectrin glycation and thus maintain their optimal membrane function during their long circulatory life span
CD45 lateral mobility is regulated by the spectrin-ankyrin cytoskeleton of T cells
Important region in the beta-spectrin C-terminus for association with the alpha chain and for spectrin tetramer formation is defined.
The spectrin-ankyrin skeleton controls CD45 surface display and interleukin-2 production
the repeats of five human beta-spectrins have been analysed
This study identifies the precise sites of all significant phosphorylation events on beta-spectrin and has determined that these phosphorylation events apparently occur in a tightly regulated sequential order.
analysis of erythroid alpha and beta spectrin chaperone activity and prodan binding
Binding sites for both protein 4.1R and actin are located in both of the beta I-spectrin calponin homology domains, (CH1 and CH2).
analysis of conformational stabilities of the structural repeats of erythroid spectrin
This locus encodes a member of the spectrin gene family. Spectrin proteins, along with ankyrin, play a role in cell membrane organization and stability. The protein encoded by this locus functions in stability of erythrocyte membranes, and mutations in this gene have been associated with spherocytosis type 2, hereditary elliptocytosis, and neonatal hemolytic anemia. Alternatively spliced transcript variants have been described.
spectrin, beta, erythrocytic
, spectrin beta
, spectrin, beta, erythrocytic (includes spherocytosis, clinical type I)
, spectrin beta chain, erythrocyte
, beta-I spectrin
, beta-spectrin 1
, brain erythroid spectrin (235E)
, spectrin R
, spectrin beta 1
, spectrin beta chain, erythrocytic
, membrane cytoskeletal protein
, erythroid spectrin beta