Browse our Shwachman-Bodian-Diamond Syndrome (SBDS) ELISA Kits

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Shwachman-Bodian-Diamond Syndrome ELISA Kits (SBDS)
On are 5 Shwachman-Bodian-Diamond Syndrome (SBDS) ELISA Kits from 1 different suppliers available. Additionally we are shipping Shwachman-Bodian-Diamond Syndrome Antibodies (46) and Shwachman-Bodian-Diamond Syndrome Proteins (16) and many more products for this protein. A total of 71 Shwachman-Bodian-Diamond Syndrome products are currently listed.
4733401P19Rik, AI836084, CGI-97, SDS, SWDS, zgc:56700

Shwachman-Bodian-Diamond Syndrome (SBDS) ELISA Kits by Reactivity

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More ELISA Kits for Shwachman-Bodian-Diamond Syndrome Interaction Partners

Zebrafish Shwachman-Bodian-Diamond Syndrome (SBDS) interaction partners

  1. Knockdown of the zebrafish sbds ortholog fully recapitulates the spectrum of developmental abnormalities observed in the human Shwachman-Bodian-Diamond syndrome.

  2. The sbds gene function is essential for normal pancreas and myeloid development in zebrafish. Zebrafish is a model system to study sbds gene function and for evaluation of novel therapies for Shwachman-Diamond syndrome.

Human Shwachman-Bodian-Diamond Syndrome (SBDS) interaction partners

  1. SBDS function is specifically required for efficient translation re-initiation into the protein isoforms C/EBPalpha (show CEBPA ELISA Kits)-p30 (show CENPV ELISA Kits) and C/EBPbeta (show CEBPB ELISA Kits)-LIP, which is controlled by a single cis (show CISH ELISA Kits)-regulatory upstream open reading frame (uORF) in the 5' untranslated regions (5' UTRs) of both mRNAs.

  2. Association of EFL1 (show EFNA1 ELISA Kits) to SBDS did not modify the affinity for GTP (show AK3 ELISA Kits) but dramatically decreased that for GDP by increasing the dissociation rate of the nucleotide.

  3. The clinical diagnosis was confirmed by detection of compound heterozygous mutations in SBDS using whole-exome sequencing: a recurrent intronic mutation causing aberrant splicing (c.258+2T>C) and a novel missense variant in a highly conserved codon (c.41A>G, p.Asn14Ser), considered to be damaging for the protein structure by in silico prediction programs

  4. Upon EFL1 (show EFNA1 ELISA Kits) binding, SBDS is repositioned around helix 69, thus facilitating a conformational switch in EFL1 (show EFNA1 ELISA Kits) that displaces eIF6 (show EIF6 ELISA Kits) by competing for an overlapping binding site on the 60S ribosomal subunit.

  5. Genetic variations in exon 2 of SBDS gene do not appear to be contributing to aplastic anemia in the north Indian population.

  6. The interaction between EFL1 (show EFNA1 ELISA Kits) and SBDS was analyzed by size exclusion chromatography, gel shift assay, and isothermal titration calorimetry. The results showed that EFL1 (show EFNA1 ELISA Kits) interacted directly with SBDS.

  7. SBDS protein acts as a nucleotide exchange factor that stabilizes binding to GTP (show AK3 ELISA Kits) for human GTPase (show RACGAP1 ELISA Kits).

  8. Lack of mutation in exon 2 of sbds protein in acute myeloid leukemia (show BCL11A ELISA Kits) suggests this subset is unlikely to have underlying sds (show SDS ELISA Kits)

  9. We conclude that knockdown of SBDS leads to growth inhibition and defects in ribosome maturation

  10. SBDS protein facilitates the release of eIF6 (show EIF6 ELISA Kits), a factor that prevents ribosome joining.

Mouse (Murine) Shwachman-Bodian-Diamond Syndrome (SBDS) interaction partners

  1. Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes

  2. Sbds genotypes correlated with phenotypes in a mouse model of Shwachman-Diamond syndrome. Defects developed specifically in the pancreata of mice, reducing growth of mice and production of digestive enzymes.

  3. Sbds is required for osteoclastogenesis by regulating monocyte migration via Rac2 (show RAC2 ELISA Kits) and osteoclast differentiation signaling downstream of RANK.

  4. Sbds is an essential gene for early mammalian development, with an expression pattern consistent with a critical role in cell proliferation.

  5. loss of Sbds is sufficient to induce abnormalities in hematopoiesis

  6. The majority of Shwachman-Diamond syndrome cases are results of mutations in SBDS gene on chromosone 7q11.

Shwachman-Bodian-Diamond Syndrome (SBDS) Antigen Profile

Antigen Summary

This gene encodes a member of a highly conserved protein family that exists from archaea to vertebrates and plants. The encoded protein may function in RNA metabolism. Mutations within this gene are associated with Shwachman-Bodian-Diamond syndrome. An alternative transcript has been described, but its biological nature has not been determined. This gene has a closely linked pseudogene that is distally located.

Alternative names and synonyms associated with Shwachman-Bodian-Diamond Syndrome (SBDS)

  • Shwachman-Bodian-Diamond syndrome (sbds) Elisa Kit
  • shwachman-Bodian-Diamond syndrome (LOAG_04440) Elisa Kit
  • Shwachman-Bodian-Diamond syndrome (SBDS) Elisa Kit
  • Shwachman-Bodian-Diamond syndrome (Sbds) Elisa Kit
  • Shwachman-Bodian-Diamond syndrome homolog (human) (Sbds) Elisa Kit
  • 4733401P19Rik Elisa Kit
  • AI836084 Elisa Kit
  • CGI-97 Elisa Kit
  • SDS Elisa Kit
  • SWDS Elisa Kit
  • zgc:56700 Elisa Kit

Protein level used designations for SBDS

ribosome maturation protein SBDS , shwachman-Bodian-Diamond syndrome protein homolog , shwachman-Bodian-Diamond syndrome , Shwachman-Bodian-Diamond syndrome homolog , protein 22A3

448365 Xenopus (Silurana) tropicalis
9941848 Loa loa
394096 Danio rerio
100049749 Xenopus laevis
417477 Gallus gallus
51119 Homo sapiens
607017 Canis lupus familiaris
513237 Bos taurus
288615 Rattus norvegicus
100172536 Pongo abelii
66711 Mus musculus
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