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SMC1α Antibody (H-6): sc-393171

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Datasheets
  • SMC1α Antibody (H-6) is a mouse monoclonal IgG3 κ SMC1α antibody, cited in 3 publications, provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 1202-1233 at the C-terminus of SMC1a of human origin
  • recommended for detection of SMC1α of mouse, rat, human and avian origin by WB, IP, IF and ELISA; also reactive with additional species, including and equine, canine, bovine, porcine and avian
  • TransCruz reagent for ChIP application (sc-393171 X, 200 µg/0.1 ml)
  • m-IgG3 BP-HRP is the preferred secondary detection reagent for SMC1α Antibody (H-6) for WB applications. This reagent is now offered in a bundle with SMC1α Antibody (H-6) (see ordering information below).
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SMC1α Antibody (H-6) is a mouse monoclonal IgG3 kappa light chain antibody that detects SMC1α protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-SMC1α antibody (H-6) is available as the non-conjugated form. SMC1α protein, also known as structural maintenance of chromosomes protein 1A, plays a crucial role in maintaining chromosome integrity during cell division. SMC1α protein is a 1,233 amino acid nuclear protein essential for sister chromatid cohesion, a process ensuring accurate chromosome segregation during mitosis. SMC1α protein is part of the cohesion complex, which is vital for holding sister chromatids together after DNA replication, thereby preventing aneuploidy and ensuring genomic stability. Additionally, SMC1α protein interacts with key proteins such as BRCA1, and SMC1α phosphorylation by ATM suggests significant involvement in DNA damage repair mechanisms. Mutations in the gene encoding SMC1α have been linked to Cornelia de Lange syndrome, a developmental disorder characterized by various physical and cognitive challenges. Anti-SMC1α antibody (H-6) effectively detects this important protein, making SMC1α monoclonal antibody (H-6) a valuable tool for researchers studying cell cycle regulation and related genetic disorders.

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

SMC1α Antibody (H-6) References:

  1. Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes (SMC) family.  |  Nishiwaki, T., et al. 1999. J Hum Genet. 44: 197-202. PMID: 10319587
  2. Structural maintenance of chromosomes (SMC) proteins: conserved molecular properties for multiple biological functions.  |  Strunnikov, AV. and Jessberger, R. 1999. Eur J Biochem. 263: 6-13. PMID: 10429180
  3. Differential association of SMC1alpha and SMC3 proteins with meiotic chromosomes in wild-type and SPO11-deficient male mice.  |  James, RD., et al. 2002. Chromosome Res. 10: 549-60. PMID: 12498344
  4. Temporally and spatially selective loss of Rec8 protein from meiotic chromosomes during mammalian meiosis.  |  Lee, J., et al. 2003. J Cell Sci. 116: 2781-90. PMID: 12759374
  5. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.  |  Deardorff, MA., et al. 2007. Am J Hum Genet. 80: 485-94. PMID: 17273969
  6. Chromosome elimination in the interspecific hybrid medaka between Oryzias latipes and O. hubbsi.  |  Sakai, C., et al. 2007. Chromosome Res. 15: 697-709. PMID: 17603754
  7. Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.  |  Revenkova, E., et al. 2009. Hum Mol Genet. 18: 418-27. PMID: 18996922
  8. Cornelia de Lange syndrome, cohesin, and beyond.  |  Liu, J. and Krantz, ID. 2009. Clin Genet. 76: 303-14. PMID: 19793304
  9. Spectrum and consequences of SMC1A mutations: the unexpected involvement of a core component of cohesin in human disease.  |  Mannini, L., et al. 2010. Hum Mutat. 31: 5-10. PMID: 19842212
  10. Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome.  |  Olioso, G., et al. 2009. Am J Med Genet A. 149A: 2532-7. PMID: 19876900
  11. SMC1: an essential yeast gene encoding a putative head-rod-tail protein is required for nuclear division and defines a new ubiquitous protein family.  |  Strunnikov, AV., et al. 1993. J Cell Biol. 123: 1635-48. PMID: 8276886
  12. Identification of two distinct human SMC protein complexes involved in mitotic chromosome dynamics.  |  Schmiesing, JA., et al. 1998. Proc Natl Acad Sci U S A. 95: 12906-11. PMID: 9789013

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SMC1α Antibody (H-6)

sc-393171
200 µg/ml
$322.00

SMC1α Antibody (H-6): m-IgG3 BP-HRP Bundle

sc-550594
200 µg Ab; 40 µg BP
$361.00

SMC1α (H-6) Neutralizing Peptide

sc-393171 P
100 µg/0.5 ml
$69.00

SMC1α Antibody (H-6) X

sc-393171 X
200 µg/0.1 ml
$322.00

What application is the blocking peptide sc-393171 P appropriate for?

Asked by: jenniferc
Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
Answered by: Technical Support
Date published: 2017-02-25
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Rated 5 out of 5 by from 抗体量太少啦说是10ul的抗体,到货后离心只有1微升,什么都没有做起来,上一支抗体足足10ul,而且效果很好,如果这支可以重新寄就太完美了
Date published: 2017-10-19
Rated 5 out of 5 by from Great Western blot data of SMC1 expression in KGreat Western blot data of SMC1 expression in K-562, Jurkat, U-937, NIH/3T3, MOLT-4 and HL-60 nuclear extracts. -SCBT QC
Date published: 2013-10-18
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SMC1α Antibody (H-6) is rated 5.0 out of 5 by 2.
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