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OP16L Anti-c-ErbB2/c-Neu (Ab-4) Mouse mAb (7.16.4)

Anti-c-ErbB2/c-Neu (Ab-4), mouse monoclonal, clone 7.16.4, recognizes the ~185 kDa c-ErbB2/c-Neu in overexpressing B104-1-1 cells. It is validated for WB, ICC, IP, and IHC with frozen sections.

Anti-c-ErbB2/c-Neu (Ab-4) Mouse mAb (7.16.4) MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: Anti-HER2, Anti-Neu, Anti-ErbB2, Anti-Erythroblastosis Virus

OP16L
Purchase on Sigma-Aldrich

Přehled

Replacement Information

Tabulka spec. kláve

Species ReactivityHostAntibody Type
H, RMMonoclonal Antibody

Products

Katalogové čísloBalení ks/bal.
OP16L-100UG Skleněná láhev 100 μg
OP16L-500UG Skleněná láhev 500 μg
Description
OverviewRecognizes the ~185 kDa c-ErbB2/c-Neu protein in overexpressing B104-1-1 cells.
Catalogue NumberOP16L
Brand Family Calbiochem®
SynonymsAnti-HER2, Anti-Neu, Anti-ErbB2, Anti-Erythroblastosis Virus
References
ReferencesZhang, H., et al. 1999. Exp. Mol. Pathol. 67, 15.
Peterson, N.C. and Greene, M.I., 1988. DNA Cell Biol. 17, 1031.
Kokai, Y., et al. 1988. Proc. Natl. Acad. Sci. USA 85, 5389.
Van De Vijver, M.J., et al. 1988. New Engl. J. Med. 319, 1239.
DiFiore, P.P., et al. 1987. Science 237, 178.
Kokai, Y., et al. 1987. Proc. Natl. Acad. Sci. USA 84, 8498.
Slamon, D.J., et al. Science 235, 177.
Varley, J.M., et al. 1987. Oncogene 1, 423.
Bargmann, C.I., et al. 1986. Nature 319, 226.
Yamamoto, T., et al. 1986. Nature 319, 230.
Blick, M., et al. 1984. Blood 64, 1234.
Schwab, M., et al. 1984. Cold Spring Harbor Laboratory 2, 215.
Product Information
FormLyophilized
FormulationLyophilized from a volatile buffer, 100 µg BSA.
Negative controlFisher rat embryo cells
Positive controlB104-1-1 cells
PreservativeNone
Quality LevelMQ100
Applications
Application ReferencesImmunoprecipitation Kokai, Y., et al. 1989. Cell 58, 287. Kokai, Y., et al. 1988. Proc. Natl. Acad. Sci. USA 85, 5389. Frozen Sections Kokai, Y., et al. 1987. Proc. Natl. Acad. Sci. USA 84, 8498. Original Clone, Growth Inhibition Assays Drebin, J.A., et al. 1988. Oncogene 2, 273. Immunoblotting Montgomery, R.B., et al. 2005. Cancer Res. 65, 650.
Key Applications Frozen Sections
Growth Inhibition Assay
Immunoblotting (Western Blotting)
Immunocytochemistry
Immunoprecipitation
Application NotesGrowth Inhibition Assays (see application references)
Frozen Sections (5 µg/ml, see application references)
Immunoblotting (see application references)
Immunocytochemistry (5 µg/ml)
Immunoprecipitation (1 µg/ml, see application references)
Application CommentsStains frozen tissue sections of rat cells overexpressing the c-neu protein. This antibody does not inhibit in vitro protein-tyrosine kinase activity, but it will inhibit in vivo growth of tumors overexpressing the neu oncogene (see application references). Does not cross-react with the EGF receptor. Antibody should be titrated for optimal results in individual systems.
Biological Information
ImmunogenB104-1-1 cells overexpressing rat c-ErbB2/c-Neu
ImmunogenHuman
Epitopewithin the extracellular domain
Clone7.16.4
HostMouse
IsotypeIgG2a
Species Reactivity
  • Human
  • Rat
Antibody TypeMonoclonal Antibody
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Do not freeze Ok to freeze
Special InstructionsReconstitute the lyophilized antibody with sterile PBS, pH 7.4, or sterile 20 mM Tris-saline (20 mM Tris containing 0.15 M NaCl), pH 7.4, to yield a final concentration of 100 µg/ml. Lyophilized antibodies should be reconstituted at 4°C with occasional gentle mixing for at least 2 h. Following reconstitution, refrigerate (4°C) for short-term storage or aliquot and freeze (-20°C) for long-term storage with 0.1% azide. Avoid freeze/thaw cycles of solutions.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Katalogové číslo GTIN
OP16L-100UG 04055977208733
OP16L-500UG 04055977208740

Documentation

Anti-c-ErbB2/c-Neu (Ab-4) Mouse mAb (7.16.4) Certificates of Analysis

TitleLot Number
OP16L

References

Přehled odkazů
Zhang, H., et al. 1999. Exp. Mol. Pathol. 67, 15.
Peterson, N.C. and Greene, M.I., 1988. DNA Cell Biol. 17, 1031.
Kokai, Y., et al. 1988. Proc. Natl. Acad. Sci. USA 85, 5389.
Van De Vijver, M.J., et al. 1988. New Engl. J. Med. 319, 1239.
DiFiore, P.P., et al. 1987. Science 237, 178.
Kokai, Y., et al. 1987. Proc. Natl. Acad. Sci. USA 84, 8498.
Slamon, D.J., et al. Science 235, 177.
Varley, J.M., et al. 1987. Oncogene 1, 423.
Bargmann, C.I., et al. 1986. Nature 319, 226.
Yamamoto, T., et al. 1986. Nature 319, 230.
Blick, M., et al. 1984. Blood 64, 1234.
Schwab, M., et al. 1984. Cold Spring Harbor Laboratory 2, 215.

Citations

Název
  • R. Bruce Montgomery, et al. (2005) Endogenous Anti-HER2 Antibodies Block HER2 Phosphorylation and Signaling through Extracellular Signal-Regulated Kinase. Cancer Research 65, 650-656.
    		•
    Data Sheet

    Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

    Revision16-November-2007 JSW
    SynonymsAnti-HER2, Anti-Neu, Anti-ErbB2, Anti-Erythroblastosis Virus
    ApplicationGrowth Inhibition Assays (see application references)
    Frozen Sections (5 µg/ml, see application references)
    Immunoblotting (see application references)
    Immunocytochemistry (5 µg/ml)
    Immunoprecipitation (1 µg/ml, see application references)
    DescriptionPurified mouse monoclonal antibody generated by immunizing C3H mice with the specified immunogen and fusing splenocytes with NS-1 mouse myeloma cells (see application references). Recognizes the ~185 kDa c-Erb2/c-neu protein.
    BackgroundAmplification of the human proto-oncogene c-neu occurs in approximately 30% of breast carcinomas and the amplification maybe a useful predictor of disease prognosis. Gene amplification and the resulting overexpression of proto-oncogene encoded proteins is thought to transform cells by chronically stimulating signal transduction pathways and in model systems overexpression of human c-neu induces cellular transformation. In the rat model system, a point mutation has been located within the transmembrane domain of the c-neu oncogene. neu (from neuroglioblastomas) is also referred to as erbB-2 (from erythroblastosis virus) and HER2 (for Human Epidermal Growth Factor Receptor) and was the second of four members of the EGF receptor family to be described.
    HostMouse
    Immunogen speciesHuman
    ImmunogenB104-1-1 cells overexpressing rat c-ErbB2/c-Neu
    Epitopewithin the extracellular domain
    Clone7.16.4
    IsotypeIgG2a
    Specieshuman, rat
    Positive controlB104-1-1 cells
    Negative controlFisher rat embryo cells
    FormLyophilized
    FormulationLyophilized from a volatile buffer, 100 µg BSA.
    PreservativeNone
    CommentsStains frozen tissue sections of rat cells overexpressing the c-neu protein. This antibody does not inhibit in vitro protein-tyrosine kinase activity, but it will inhibit in vivo growth of tumors overexpressing the neu oncogene (see application references). Does not cross-react with the EGF receptor. Antibody should be titrated for optimal results in individual systems.
    Storage +2°C to +8°C
    Do Not Freeze Ok to freeze
    Special InstructionsReconstitute the lyophilized antibody with sterile PBS, pH 7.4, or sterile 20 mM Tris-saline (20 mM Tris containing 0.15 M NaCl), pH 7.4, to yield a final concentration of 100 µg/ml. Lyophilized antibodies should be reconstituted at 4°C with occasional gentle mixing for at least 2 h. Following reconstitution, refrigerate (4°C) for short-term storage or aliquot and freeze (-20°C) for long-term storage with 0.1% azide. Avoid freeze/thaw cycles of solutions.
    Toxicity Standard Handling
    ReferencesZhang, H., et al. 1999. Exp. Mol. Pathol. 67, 15.
    Peterson, N.C. and Greene, M.I., 1988. DNA Cell Biol. 17, 1031.
    Kokai, Y., et al. 1988. Proc. Natl. Acad. Sci. USA 85, 5389.
    Van De Vijver, M.J., et al. 1988. New Engl. J. Med. 319, 1239.
    DiFiore, P.P., et al. 1987. Science 237, 178.
    Kokai, Y., et al. 1987. Proc. Natl. Acad. Sci. USA 84, 8498.
    Slamon, D.J., et al. Science 235, 177.
    Varley, J.M., et al. 1987. Oncogene 1, 423.
    Bargmann, C.I., et al. 1986. Nature 319, 226.
    Yamamoto, T., et al. 1986. Nature 319, 230.
    Blick, M., et al. 1984. Blood 64, 1234.
    Schwab, M., et al. 1984. Cold Spring Harbor Laboratory 2, 215.
    Citation
  • R. Bruce Montgomery, et al. (2005) Endogenous Anti-HER2 Antibodies Block HER2 Phosphorylation and Signaling through Extracellular Signal-Regulated Kinase. Cancer Research 65, 650-656.
    		•
    Application referencesImmunoprecipitation Kokai, Y., et al. 1989. Cell 58, 287. Kokai, Y., et al. 1988. Proc. Natl. Acad. Sci. USA 85, 5389. Frozen Sections Kokai, Y., et al. 1987. Proc. Natl. Acad. Sci. USA 84, 8498. Original Clone, Growth Inhibition Assays Drebin, J.A., et al. 1988. Oncogene 2, 273. Immunoblotting Montgomery, R.B., et al. 2005. Cancer Res. 65, 650.