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CD93 antibody

The Mouse Monoclonal anti-CD93 antibody has been validated for WB, IP and FACS. It is suitable to detect CD93 in samples from Human. There are 7+ publications available.
Catalog No. ABIN967346

Quick Overview for CD93 antibody (ABIN967346)

Target

See all CD93 Antibodies
CD93

Reactivity

  • 69
  • 31
  • 30
  • 3
Human

Host

  • 53
  • 21
  • 4
  • 3
Mouse

Clonality

  • 53
  • 26
  • 1
Monoclonal

Conjugate

  • 31
  • 6
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CD93 antibody is un-conjugated

Application

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  • 6
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  • 1
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Western Blotting (WB), Immunoprecipitation (IP), Flow Cytometry (FACS)

Clone

R3
  • Brand

    BD Pharmingen™

    Characteristics

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.

    Purification

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogen

    C1q-binding protein

    Isotype

    IgM kappa
  • Application Notes

    Immunofluorescent Staining and Flow Cytometric Analysis:
    The staining technique and blocking controls are described in detail by C. Prussin and D. Metcalfe. A suitable mouse IgM, kappa isotype control for assessing the level of background staining on human cells is recommended: use at comparable concentrations to antibody of interest (eg, Less or equal than 0.5 µg Ab/1 million cells) (see Figure).

    Western Blotting and immunoprecipitation:
    When run under non-reducing conditions, Human C1qRp migrates as a 100 kDa protein, due to high level of glycosylation C1qR migrates as 126 kDa under reducing conditions. The R3 antibody is suitable to detect C1qRp by Western blotting and immunprecipitation as described, however, the antibody is not tested for this application. Reactivity of the antibody with the reduced protein is dramatically decreased.

    Modulation of monocyte phagocytic activity:
    Pretreatment of monocytes with R3 neutralizes C1q-mediated enhancement of phagocytosis. In addition, when immobilized, R3 mimics C1q- MBL- or SPA-mediated enhancement of phagocytosis, however, the antibody is not tested for this application.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Aqueous buffered solution containing ≤0.09 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Storage Comment

    Store undiluted at 4°C.
  • Danet, Luongo, Butler, Lu, Tenner, Simon, Bonnet: "C1qRp defines a new human stem cell population with hematopoietic and hepatic potential." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, Issue 16, pp. 10441-5, (2002) (PubMed).

    Nepomuceno, Ruiz, Park, Tenner: "C1qRP is a heavily O-glycosylated cell surface protein involved in the regulation of phagocytic activity." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 162, Issue 6, pp. 3583-9, (1999) (PubMed).

    Tenner: "C1q receptors: regulating specific functions of phagocytic cells." in: Immunobiology, Vol. 199, Issue 2, pp. 250-64, (1999) (PubMed).

    Nepomuceno, Tenner: "C1qRP, the C1q receptor that enhances phagocytosis, is detected specifically in human cells of myeloid lineage, endothelial cells, and platelets." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 160, Issue 4, pp. 1929-35, (1998) (PubMed).

    Nepomuceno, Henschen-Edman, Burgess, Tenner: "cDNA cloning and primary structure analysis of C1qR(P), the human C1q/MBL/SPA receptor that mediates enhanced phagocytosis in vitro." in: Immunity, Vol. 6, Issue 2, pp. 119-29, (1997) (PubMed).

    Guan, Robinson, Goodman, Tenner: "Cell-surface protein identified on phagocytic cells modulates the C1q-mediated enhancement of phagocytosis." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 152, Issue 8, pp. 4005-16, (1994) (PubMed).

    Guan, Burgess, Robinson, Goodman, McTigue, Tenner: "Phagocytic cell molecules that bind the collagen-like region of C1q. Involvement in the C1q-mediated enhancement of phagocytosis." in: The Journal of biological chemistry, Vol. 266, Issue 30, pp. 20345-55, (1991) (PubMed).

  • Target

    CD93

    Alternative Name

    CDw93

    Background

    The immunogen used to raise R3 was C1q-binding protein preparation as described. Human C1qRp is a 631 a.a. protein (~66.5 kD) protein that is highly expressed on monocytes/macrophages, neutrophil granulocytes but not on T and B lymphocytes. C1qRp binds C1q, the recognition subunit of the first component (C1) of the complement pathway, as well as MBL (Mannose-binding-lectin) and SPA (Pulmonary Surfactant Protein A). Human C1qRp is involved in the C1q-mediated enhancement of phagocytosis. R3 is suitable to detect C1qRp expression on cells of myeloid lineage by flow cytometry, C1qRp in cellular lysates by Western blotting or immunoprecipitation. Pretreatment of monocytes with R3 neutralizes C1q-mediated enhancement of phagocytosis. In addition, when immobilized, R3 mimics C1q- MBL- or SPA-mediated enhancement of phagocytosis as reported.
    CDw93 (C1qRp) has been reported to define a human stem cell population with hematopoietic and hepatic potential.
    Synonyms: C1qRp
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