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The protein encoded by SEC23B is a member of the SEC23 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. Additionally we are shipping Sec23 Homolog B (S. Cerevisiae) Antibodies (38) and Sec23 Homolog B (S. Cerevisiae) Kits (4) and many more products for this protein.
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described the functional interaction between GATA1 (show GATA1 Proteins) and SEC23B genes in two patients with suspected congenital dyserythropoietic anemia type II
these data demonstrate an equivalent function for SEC23A (show SEC23A Proteins)/B, with evolutionary shifts in the transcription program likely accounting for the distinct phenotypes of SEC23A (show SEC23A Proteins)/B deficiency within and across species, a paradigm potentially applicable to other sets of paralogous genes.
novel compound mutations of c.1727T>C and c.1831C>T of the SEC23B gene probably underlie the congenital dyserythropoietic anemia type II in the family
Mutation in SEC23B gene is associated with congenital dyserythropoietic anemia.
miR (show MLXIP Proteins)-130a is an epigenetically regulated miRNA involved in regulation of key molecular and phenotypic features of prostate carcinogenesis, acting as a tumour suppressor miRNA by targeting SEC23B and DEPDC1 (show DEPDC1 Proteins).
SEC23B-Y462C congenital dyserythropoietic anemia type II is only seen in a distinct Indian community (Vaish) in whom a recessively inherited shared haplotype can be showed, consistent with a founder effect.
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.
Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A --> G mutation, and pseudo-Gaucher cells in two siblings has been described.
ALG-2 (show PDCD6 Proteins) attenuates COPII budding in vitro and stabilizes the Sec23/Sec31A (show SEC31A Proteins) complex.
Both probands with congenital dyserythropoietic anemia IotaI in the second family were homozygotes of the SEC23B gene with mutation c.938G>A (R313H).
SEC23B but not SEC23A (show SEC23A Proteins) is essential for murine pancreatic development.
Acinar Sec23b deletion results in induction of ER stress and increased apoptosis in the pancreas, potentially explaining the loss of pancreatic cells and decreased pancreatic weight. These findings demonstrate that SEC23B is required for normal function of pancreatic acinar cells in adult mice.
Results show that transplantation of SEC23B-deficient hematopoietic stem cells does not result in a hematopoietic stem cells phenotype.
In SEC23B-deficient embryonic pancreas, defects occur in exocrine and endocrine tissues shortly after differentiation.
The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The function of this gene product has been implicated in cargo selection and concentration. Multiple alternatively spliced transcript variants have been identified in this gene.
SEC23-like protein B
, SEC23-related protein B
, protein transport protein Sec23B
, transport protein SEC23B
, SEC23-related protein A
, protein transport protein Sec23A