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SBDS Antibody (D-9): sc-271350

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Datasheets
  • SBDS Antibody (D-9) is a mouse monoclonal IgG1 κ SBDS antibody, cited in 3 publications, provided at 200 µg/ml
  • raised against amino acids 1-250 representing full length SBDS of human origin
  • SBDS Antibody (D-9) is recommended for detection of SBDS of mouse, rat and human origin by WB, IP, IF and ELISA
  • Anti-SBDS Antibody (D-9) is available conjugated to agarose for IP; HRP for WB, IHC(P) and ELISA; and to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • also available conjugated to Alexa Fluor® 488, Alexa Fluor® 546, Alexa Fluor® 594 or Alexa Fluor® 647 for WB (RGB), IF, IHC(P) and FCM, and for use with RGB fluorescent imaging systems, such as iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • also available conjugated to Alexa Fluor® 680 or Alexa Fluor® 790 for WB (NIR), IF and FCM; for use with Near-Infrared (NIR) detection systems, such as LI-COR®Odyssey®, iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for SBDS Antibody (D-9). This work is in progress.
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SBDS Antibody (D-9) is a mouse monoclonal IgG1 kappa light chain antibody that detects SBDS protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). SBDS (D-9) antibody is available in both non-conjugated and various conjugated forms, including agarose, horseradish peroxidase (HRP), phycoerythrin (PE), fluorescein isothiocyanate (FITC), and multiple Alexa Fluor® conjugates. The Shwachman-Bodian-Diamond syndrome (SBDS) protein, consisting of 249 amino acids, is a member of the UPF0023 family and plays a crucial role in RNA metabolism, which is essential for proper cellular function and gene expression. SBDS protein is predominantly located in the cytoplasm, where SBDS participates in ribosome biogenesis and the regulation of mRNA decay, highlighting its importance in maintaining cellular homeostasis. Notably, mutations in the SBDS gene lead to Shwachman-Diamond syndrome, an autosomal recessive disorder characterized by hematologic dysfunction, skeletal abnormalities, and pancreatic exocrine insufficiency, as well as an increased risk of leukemia and myelodysplasia in affected individuals. The structural features of SBDS, including its C-terminal domain with a ferredoxin-like fold and RNA-binding capabilities, along with its central three-helical bundle and N-terminal domain, are critical for its function and interaction with other proteins involved in RNA processing.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

SBDS Antibody (D-9) References:

  1. Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome.  |  Shammas, C., et al. 2005. J Biol Chem. 280: 19221-9. PMID: 15701631
  2. The Shwachman-Bodian-Diamond syndrome protein family is involved in RNA metabolism.  |  Savchenko, A., et al. 2005. J Biol Chem. 280: 19213-20. PMID: 15701634
  3. Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship.  |  Kuijpers, TW., et al. 2005. Blood. 106: 356-61. PMID: 15769891
  4. Identification of novel mutations in patients with Shwachman-Diamond syndrome.  |  Nicolis, E., et al. 2005. Hum Mutat. 25: 410. PMID: 15776428
  5. The Shwachman-Diamond SBDS protein localizes to the nucleolus.  |  Austin, KM., et al. 2005. Blood. 106: 1253-8. PMID: 15860664
  6. Genetic analysis of Shwachman-Diamond syndrome: phenotypic heterogeneity in patients carrying identical SBDS mutations.  |  Kawakami, T., et al. 2005. Tohoku J Exp Med. 206: 253-9. PMID: 15942154
  7. Mutation analysis of SBDS in pediatric acute myeloblastic leukemia.  |  Majeed, F., et al. 2005. Pediatr Blood Cancer. 45: 920-4. PMID: 16007594
  8. Shwachman-Diamond syndrome.  |  Dror, Y. 2005. Pediatr Blood Cancer. 45: 892-901. PMID: 16047374
  9. Identification of a novel AluSx-mediated deletion of exon 3 in the SBDS gene in a patient with Shwachman-Diamond syndrome.  |  Costa, E., et al. 2007. Blood Cells Mol Dis. 39: 96-101. PMID: 17376717

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SBDS Antibody (D-9)

sc-271350
200 µg/ml
$322.00

SBDS Antibody (D-9) AC

sc-271350 AC
500 µg/ml, 25% agarose
$424.00

SBDS Antibody (D-9) HRP

sc-271350 HRP
200 µg/ml
$322.00

SBDS Antibody (D-9) FITC

sc-271350 FITC
200 µg/ml
$336.00

SBDS Antibody (D-9) PE

sc-271350 PE
200 µg/ml
$349.00

SBDS Antibody (D-9) Alexa Fluor® 488

sc-271350 AF488
200 µg/ml
$364.00

SBDS Antibody (D-9) Alexa Fluor® 546

sc-271350 AF546
200 µg/ml
$364.00

SBDS Antibody (D-9) Alexa Fluor® 594

sc-271350 AF594
200 µg/ml
$364.00

SBDS Antibody (D-9) Alexa Fluor® 647

sc-271350 AF647
200 µg/ml
$364.00

SBDS Antibody (D-9) Alexa Fluor® 680

sc-271350 AF680
200 µg/ml
$364.00

SBDS Antibody (D-9) Alexa Fluor® 790

sc-271350 AF790
200 µg/ml
$364.00

I need to use an antibody to detect the protein in samples of monkey origin. Do you know if sc-271350: SBDS (D-9) mouse monoclonal antibody will work?

Asked by: Dr Ninau Qelp
Please contact our Technical Service Department and we would be happy to perform sequence analysis and review our data to answer any questions you may have about additional species reactivity.
Answered by: Technical Support
Date published: 2017-03-06
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Rated 5 out of 5 by from Produced nice Western blot data of SBDS expressionProduced nice Western blot data of SBDS expression in NIH/3T3 and HeLa whole cell lysates. -SCBT QC
Date published: 2013-08-05
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SBDS Antibody (D-9) is rated 5.0 out of 5 by 1.
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