Product Name
SBDS, Blocking Peptide
Full Product Name
SBDS Peptide
Product Gene Name
SBDS blocking peptide
[Similar Products]
Product Synonym Gene Name
CGI-97; FLJ10917; SDS; SWDS[Similar Products]
SBDS peptide (MBS3232850) is used for blocking the activity of SBDS antibody (MBS3207885)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q9Y3A5
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of SBDS blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
SBDS blocking peptide
This is a synthetic peptide designed for use in combination with anti-SBDS antibody made
Target Description: SBDS is a member of a highly conserved protein family that exists from archaea to vertebrates and plants. The protein may function in RNA metabolism. Mutations within its gene are associated with Shwachman-Bodian-Diamond syndrome.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.
Product Categories/Family for SBDS blocking peptide
Peptide
Applications Tested/Suitable for SBDS blocking peptide
Immunohistochemistry (IHC), Western Blot (WB)
NCBI/Uniprot data below describe general gene information for SBDS. It may not necessarily be applicable to this product.
NCBI Accession #
NP_057122
[Other Products]
NCBI GenBank Nucleotide #
NM_016038
[Other Products]
UniProt Primary Accession #
Q9Y3A5
[Other Products]
UniProt Related Accession #
Q9Y3A5[Other Products]
NCBI Official Full Name
ribosome maturation protein SBDS
NCBI Official Synonym Full Names
SBDS ribosome maturation factor
NCBI Official Symbol
SBDS??[Similar Products]
NCBI Official Synonym Symbols
SDS; SWDS; CGI-97
??[Similar Products]
NCBI Protein Information
ribosome maturation protein SBDS
UniProt Protein Name
Ribosome maturation protein SBDS
UniProt Synonym Protein Names
Shwachman-Bodian-Diamond syndrome protein
Protein Family
Ribosome maturation protein
UniProt Gene Name
SBDS??[Similar Products]
UniProt Entry Name
SBDS_HUMAN
NCBI Summary for SBDS
This gene encodes a highly conserved protein that plays an essential role in ribosome biogenesis. The encoded protein interacts with elongation factor-like GTPase 1 to disassociate eukaryotic initiation factor 6 from the late cytoplasmic pre-60S ribosomal subunit allowing assembly of the 80S subunit. Mutations within this gene are associated with the autosomal recessive disorder Shwachman-Bodian-Diamond syndrome. This gene has a closely linked pseudogene that is distally located. [provided by RefSeq, Jan 2017]
UniProt Comments for SBDS
SBDS: Required for the assembly of mature ribosomes and ribosome biogenesis. Together with EFTUD1, triggers the GTP- dependent release of EIF6 from 60S pre-ribosomes in the cytoplasm, thereby activating ribosomes for translation competence by allowing 80S ribosome assembly and facilitating EIF6 recycling to the nucleus, where it is required for 60S rRNA processing and nuclear export. Required for normal levels of protein synthesis. May play a role in cellular stress resistance. May play a role in cellular response to DNA damage. May play a role in cell proliferation. Defects in SBDS are the cause of Shwachman-Diamond syndrome (SDS). SDS is an autosomal recessive disorder characterized by pancreatic exocrine insufficiency, hematologic dysfunction, and skeletal abnormalities. Belongs to the SDO1/SBDS family.
Protein type: Nucleolus
Chromosomal Location of Human Ortholog: 7q11.21
Cellular Component: nucleoplasm; spindle pole; cytoplasm; nucleolus; nucleus
Molecular Function: rRNA binding; protein binding; microtubule binding; ribosome binding
Biological Process: bone marrow development; cell proliferation; leukocyte chemotaxis; ribosomal large subunit biogenesis and assembly; mitotic spindle stabilization; inner cell mass cell proliferation; rRNA processing; mature ribosome assembly; bone mineralization
Disease: Shwachman-diamond Syndrome; Aplastic Anemia
Research Articles on SBDS
1. Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients.
Precautions
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