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Render Timestamp: 2025-01-02T12:18:36.644Z
Commit: 286c369131ceeedcf44c821941824d8d7e009e57
XML generation date: 2024-08-30 10:37:34.746
Product last modified at: 2025-01-01T09:03:51.346Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

Syndecan 1 (D4Y7H) Rabbit mAb (BSA and Azide Free) #49771

Filter:
  • WB
  • F

    Supporting Data

    REACTIVITY H
    SENSITIVITY Endogenous
    MW (kDa) 180-250, 70
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • F-Flow Cytometry 
    Species Cross-Reactivity Key:
    • H-Human 

    Product Information

    Product Usage Information

    This product is the carrier free version of product #12922. All data were generated using the same antibody clone in the standard formulation which contains BSA and glycerol.

    This formulation is ideal for use with technologies requiring specialized or custom antibody labeling, including fluorophores, metals, lanthanides, and oligonucleotides. It is not recommended for ChIP, ChIP-seq, CUT&RUN or CUT&Tag assays. If you require a carrier free formulation for chromatin profiling, please contact us. Optimal dilutions/concentrations should be determined by the end user.

    BSA and Azide Free antibodies are quality control tested by size exclusion chromatography (SEC) to determine antibody integrity.

    Formulation

    Supplied in 1X PBS (10 mM Na2HPO4, 3 mM KCl, 2 mM KH2PO4, and 140 mM NaCl (pH 7.8)). BSA and Azide Free.

    For standard formulation of this product see product #12922

    Storage

    Store at -20°C. This product will freeze at -20°C so it is recommended to aliquot into single-use vials to avoid multiple freeze/thaw cycles. A slight precipitate may be present and can be dissolved by gently vortexing. This will not interfere with antibody performance.

    Specificity / Sensitivity

    Syndecan 1 (D4Y7H) Rabbit mAb (BSA and Azide Free) recognizes endogenous levels of multimeric form of syndecan 1 protein. This antibody cross-reacts with proteins of unknown origin between 46-60 kDa in some cell lines.

    Species Reactivity:

    Human

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala294 of human syndecan 1 protein.

    Background

    Syndecans are a family of type 1 transmembrane heparan sulfate proteoglycans comprising four members in mammals (SDC1-4) (1) encoded by four syndecan genes. Syndecans are involved in embryonic development, tumorigenesis, and angiogenesis (2). The extracellular domain harbors attachment sites for heparan sulfate and chondroitin sulfate chains, facilitating interaction with an array of proteins, including a plethora of growth factors. In addition, the hydrophobic C-terminal intracellular domain can interact with proteins containing a PDZ domain (2). These interactions place syndecans as important integrators of membrane signaling (3). Syndecans undergo proteolytic cleavage causing the release of their extracellular domain (shedding), converting the membrane-bound proteins into soluble molecular effectors (4).

    Syndecan 1 (SDC1) is a specific marker for plasmacytic differentiation in hematologic disorders (5-7). This cell surface proteoglycan is also expressed in normal epithelial cells and tissues as well as various types of cancer tissues (8-11). The extracellular shed form of syndecan 1 remains soluble or accumulates in the extracellular matrix where it binds growth factors, cytokines and other extracellular matrix proteins (12,13). This binding activates signaling of bound growth factors or cytokines, which results in enhanced tumor growth, dissemination, angiogenesis, and osteolysis (14-17). As a result, the level of syndecan1 protein and its shed form may serve as prognostic factors for a list of malignancies (6,18,19). Syndecan 1 has recently been found to be a critical mediator of macropinocytosis in pancreatic cancer (20).
    1. Couchman, J.R. (2003) Nat Rev Mol Cell Biol 4, 926-37.
    2. Multhaupt, H.A. et al. (2009) J Physiol Pharmacol 60 Suppl 4, 31-8.
    3. Zimmermann, P. and David, G. (1999) FASEB J 13 Suppl, S91-S100.
    4. Manon-Jensen, T. et al. (2010) FEBS J 277, 3876-89.
    5. Chilosi, M. et al. (1999) Mod Pathol 12, 1101-6.
    6. Seidel, C. et al. (2000) Blood 95, 388-92.
    7. O'Connell, F.P. et al. (2004) Am J Clin Pathol 121, 254-63.
    8. Inki, P. and Jalkanen, M. (1996) Ann Med 28, 63-7.
    9. Matsumoto, A. et al. (1997) Int J Cancer 74, 482-91.
    10. Conejo, J.R. et al. (2000) Int J Cancer 88, 12-20.
    11. Zellweger, T. et al. (2003) Prostate 55, 20-9.
    12. Bayer-Garner, I.B. et al. (2001) Mod Pathol 14, 1052-8.
    13. Ramani, V.C. et al. (2013) FEBS J 280, 2294-306.
    14. Derksen, P.W. et al. (2002) Blood 99, 1405-10.
    15. You, W.K. and McDonald, D.M. (2008) BMB Rep 41, 833-9.
    16. Ramani, V.C. et al. (2011) J Biol Chem 286, 6490-9.
    17. Aragão, A.Z. et al. (2012) PLoS One 7, e43521.
    18. Joensuu, H. et al. (2002) Cancer Res 62, 5210-7.
    19. Lee, S.H. et al. (2013) Int J Clin Oncol (Epub ahead of print).
    20. Yao, W. et al. (2019) Nature 568, 410-414.
    For Research Use Only. Not For Use In Diagnostic Procedures.
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