Date published: 2026-5-16

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Fam148b Antibody (E-9): sc-390660

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Datasheets
  • Fam148b Antibody (E-9) is a mouse monoclonal IgM κ Fam148b antibody provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 50-71 near the N-terminus of Fam148b of mouse origin
  • recommended for detection of NLF2 of human origin, Fam148b of mouse origin and the corresponding rat homolog by WB, IP, IF and ELISA
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for Fam148b Antibody (E-9). This work is in progress.
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    Fam148b Antibody (E-9) is a mouse monoclonal IgM antibody that detects Fam148b of human, mouse, and rat origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). Anti-Fam148b antibody (E-9) is available as a non-conjugated format. Fam148b plays a crucial role in cellular signaling pathways, particularly in regulating neuronal development and function, which is essential for maintaining proper cognitive and motor functions. Disruptions in these pathways can lead to neurodevelopmental disorders, highlighting Fam148b′s importance in studying conditions like Angelman syndrome and Prader-Willi syndrome, both linked to genetic anomalies in the 15q11-q13 region of chromosome 15. Understanding Fam148b′s function can provide insights into the molecular mechanisms underlying these syndromes and may pave the way for potential therapeutic strategies.

    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

    Fam148b Antibody (E-9) References:

    1. Analysis of the DNA sequence and duplication history of human chromosome 15.  |  Zody, MC., et al. 2006. Nature. 440: 671-5. PMID: 16572171
    2. Effective gene therapy in an authentic model of Tay-Sachs-related diseases.  |  Cachón-González, MB., et al. 2006. Proc Natl Acad Sci U S A. 103: 10373-10378. PMID: 16801539
    3. Pyrimethamine as a potential pharmacological chaperone for late-onset forms of GM2 gangliosidosis.  |  Maegawa, GH., et al. 2007. J Biol Chem. 282: 9150-61. PMID: 17237499
    4. Molecular epigenetics of Angelman syndrome.  |  Lalande, M. and Calciano, MA. 2007. Cell Mol Life Sci. 64: 947-60. PMID: 17347796
    5. [The Prader-Willi syndrome].  |  Diene, G., et al. 2007. Ann Endocrinol (Paris). 68: 129-37. PMID: 17499572
    6. Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.  |  Makoff, AJ. and Flomen, RH. 2007. Genome Biol. 8: R114. PMID: 17573966
    7. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.  |  Ramirez, F. and Dietz, HC. 2007. J Cell Physiol. 213: 326-30. PMID: 17708531
    8. Extracellular control of TGFbeta signalling in vascular development and disease.  |  ten Dijke, P. and Arthur, HM. 2007. Nat Rev Mol Cell Biol. 8: 857-69. PMID: 17895899
    9. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.  |  Dupuis, J., et al. 2010. Nat Genet. 42: 105-16. PMID: 20081858
    10. The diabetogenic VPS13C/C2CD4A/C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals.  |  Grarup, N., et al. 2011. Diabetologia. 54: 789-94. PMID: 21249489
    11. Sexually dimorphic roles for the type 2 diabetes-associated C2cd4b gene in murine glucose homeostasis.  |  Mousavy Gharavy, SN., et al. 2021. Diabetologia. 64: 850-864. PMID: 33492421
    12. C2CD4B Evokes Oxidative Stress and Vascular Dysfunction via a PI3K/Akt/PKCα-Signaling Pathway.  |  Di Pietro, P., et al. 2024. Antioxidants (Basel). 13: PMID: 38247525

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    Fam148b Antibody (E-9)

    sc-390660
    200 µg/ml
    $322.00

    Fam148b (E-9) Neutralizing Peptide

    sc-390660 P
    100 µg/0.5 ml
    $69.00

    What application is the blocking peptide sc-390660 P appropriate for?

    Asked by: DefinitelyNotMatt
    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: 2017-03-01
    • y_2026, m_5, d_15, h_13CST
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    Rated 5 out of 5 by from Produced positive Western blot data of Fam148bProduced positive Western blot data of Fam148b expression in CTLL-2 whole cell lysate and RAW 264.7 nuclear extract . -SCBT QC
    Date published: 2014-06-26
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    Fam148b Antibody (E-9) is rated 5.0 out of 5 by 1.
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