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Merck
모든 사진(2)

주요 문서

SAB5500002

Sigma-Aldrich

Anti-α-Smooth Muscle Actin (ACTA2) Antibody,

rabbit monoclonal, SP171

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About This Item

UNSPSC 코드:
12352203
NACRES:
NA.41

제품명

Anti-SMA antibody, Rabbit monoclonal, clone SP171, recombinant, expressed in proprietary host, affinity isolated antibody

생물학적 소스

rabbit

Quality Level

재조합

expressed in proprietary host

결합

unconjugated

항체 형태

affinity isolated antibody

항체 생산 유형

primary antibodies

클론

SP171, monoclonal

종 반응성

human (tested)

종 반응성(상동성에 의해 예측)

rabbit, rat, bovine, chicken, mouse, pig

기술

immunoblotting: 1:50
immunohistochemistry: 1:200

동형

IgG

UniProt 수납 번호

배송 상태

wet ice

저장 온도

2-8°C

타겟 번역 후 변형

unmodified

유전자 정보

human ... ACTA2(59)

일반 설명

Smooth muscle actin-α (SMA), also known as α2-smooth muscle actin (ACTA2), is a cytoskeleton protein in smooth muscle cells. It is encoded by the gene mapped to human chromosome 10q23.31. SMA is a vascular smooth muscle specific isoform,
Smooth muscle actin-alpha (SMA) is a cytoskeleton protein in smooth muscle cells and their derived tumors such as leiomyoma and leiomyosarcoma. It is also expressed in myoepithelial cells of the breast and salivary gland, but not in fibroblasts, striated muscle, and myocardium.

면역원

Synthetic peptide near the N-terminus of human SMA protein.

애플리케이션

Anti-SMA antibody, Rabbit monoclonal has been used in:
  • western blotting
  • immunohistochemistry
  • immunofluorescence

생화학적/생리학적 작용

Smooth muscle actin-α (SMA)/ α2-smooth muscle actin (ACTA2) interacts with β-myosin heavy chain and facilitates vascular smooth muscle cell contraction. The encoded protein regulates c-MET (tyrosine-protein kinase Met) and focal adhesion kinase (FAK) expression in human lung adenocarcinoma cells, which positively and selectively mediates tumor progression. Thus, SMA can be used as a potential prognostic biomarker and/or target for treating metastatic lung adenocarcinoma. Mutation in the gene is associated with the development of patent ductus arteriosus (PDA), bicuspid aortic valve (BAV), iris flocculi, livedo reticularis, cerebrovascular accident (CVA) and stenosis of the aortic vasa vasorum. In addition, variation in the gene expression leads to thoracic aortic aneurysms and dissections (TAAD).

특징 및 장점

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

물리적 형태

0.1 ml rabbit monoclonal antibody purified by protein A/G in PBS/1% BSA buffer pH 7.6 with less than 0.1% sodium azide.

면책조항

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Epithelial-to-mesenchymal transition confers pericyte properties on cancer cells.
Shenoy A K, et al.
The Journal of Clinical Investigation, 126(11), 4174-4186 (2016)
Xia Ke et al.
The Journal of allergy and clinical immunology, 143(4), 1560-1574 (2018-09-09)
Numbers of mesenchymal stem cells (MSCs) are increased in the airways after allergen challenge. Ras homolog family member A (RhoA)/Rho-associated protein kinase 1 (ROCK) signaling is critical in determining the lineage fate of MSCs in tissue repair/remodeling. We sought to investigate
Ying-Chun Zhu et al.
International journal of molecular medicine, 40(4), 1165-1171 (2017-08-30)
Transforming growth factor-β (TGF-β) induces epithelial-mesenchymal transition (EMT) primarily via a Smad‑dependent mechanism. However, there are few studies available on TGF-β-induced EMT through the activation of non‑canonical pathways. In this study, the Cdc42-interacting protein-4 (CIP4)/partitioning-defective protein 6 (Par6) pathway was investigated in TGF-β1‑stimulated NRK-52E cells. Rat
Suppression of CIP4/Par6 attenuates TGF-β1-induced epithelial-mesenchymal transition in NRK-52E cells.
Zhu Y-C, et al.
International Journal of Molecular Medicine, 40(4), 1165-1171 (2017)
The genetics and genomics of thoracic aortic disease.
Pomianowski P and John A E
Journal of Cardiothoracic Surgery, 2(3), 271-271 (2013)

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