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298M-1

Sigma-Aldrich

Myosin, Smooth Muscle (SMMS-1) Mouse Monoclonal Antibody

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

Pricing and availability is not currently available.

biological source

mouse

Quality Level

100
500

conjugate

unconjugated

antibody form

culture supernatant

antibody product type

primary antibodies

clone

SMMS-1, monoclonal

description

For In Vitro Diagnostic Use in Select Regions (See Chart)

form

buffered aqueous solution

species reactivity

human

packaging

vial of 0.1 mL concentrate (298M-14)
vial of 0.5 mL concentrate (298M-15)
bottle of 1.0 mL predilute (298M-17)
vial of 1.0 mL concentrate (298M-16)
bottle of 7.0 mL predilute (298M-18)

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This Item
202M-9M7786SAB5500002
conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

species reactivity

human

species reactivity

human

species reactivity

guinea pig, human, pig, canine, rabbit, chicken

species reactivity

human (tested)

clone

SMMS-1, monoclonal

clone

1A4, monoclonal

clone

hSM-V, monoclonal

clone

SP171, monoclonal

biological source

mouse

biological source

mouse

biological source

mouse

biological source

rabbit

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

General description

Smooth Muscle Myosin, heavy chain (SMMS-1) is a cytoplasmic structural protein that is a major component of the contractile apparatus of the smooth muscle cells. SMMS-1 is also an amyoepithelium-associated protein. Anti-SMMS-1 is a mouse monoclonal antibody to smooth muscle myosin, a heavy chain that reacts with human visceral and vascular smooth muscle cells. The antibody also reacts with human myoepithelial cells. It is very helpful in identifying myoepithelial cells in benign sclerosing breast lesions and demonstrating their absence of invasive breast carcinomas.

Quality


IVD

IVD

IVD

RUO

Linkage

Myosin, Smooth Muscle Positive Control Slides, Product No. 298S, are available for immunohistochemistry (formalin-fixed, paraffin-embedded sections).

Physical form

Solution in Tris Buffer, pH 7.3-7.7, with 1% BSA and <0.1% Sodium Azide

Preparation Note

Download the IFU specific to your product lot and formatNote: This requires a keycode which can be found on your packaging or product label.

Other Notes

For Technical Service please contact: 800-665-7284 or email: service@cellmarque.com

Legal Information

Cell Marque is a trademark of Merck KGaA, Darmstadt, Germany

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    Nikolay K Popnikolov et al.
    American journal of clinical pathology, 120(2), 161-167 (2003-08-23)
    We immunohistochemically compared benign myoepithelial tumors (adenomyoepitheliomas [AMEs]) and metaplastic matrix-producing (MMP-CA) and spindle cell (MSC-CA) carcinomas of the breast to identify helpful diagnostic markers. Normal myoepithelial cells (MECs) consistently expressed cytokeratin, alpha-smooth muscle actin (SMA), myosin, S-100, CD10, and
    S N Agoff et al.
    Applied immunohistochemistry & molecular morphology : AIMM, 9(2), 164-169 (2001-06-09)
    Distinguishing low grade endometrial stromal sarcoma (ESS) from benign smooth muscle proliferations like cellular leiomyoma (CL) can be problematic; because of differing treatments and prognosis, this distinction is important. The authors tested the hypothesis that low grade ESS could be
    Robert W Werling et al.
    The American journal of surgical pathology, 27(1), 82-90 (2002-12-28)
    Identification of myoepithelial cells using antibodies to cytoskeletal proteins, such as smooth muscle myosin heavy chain (SMM-HC) and calponin, can play an important role in distinguishing invasive carcinoma from its histologic mimics. However, antibodies to these proteins may also cross-react
    D Lazard et al.
    Proceedings of the National Academy of Sciences of the United States of America, 90(3), 999-1003 (1993-02-01)
    The expression of several differentiation markers in normal human mammary gland myoepithelium and in certain stromal fibroblasts ("myofibroblasts") associated with breast carcinomas was studied by immunofluorescence microscopy of frozen sections. Several antibodies to smooth muscle-specific proteins (smooth muscle alpha-actin, smooth

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