RevMab

anti-ACTA2, Rabbit Monoclonal (RM253)

CHF 459.00
In stock
REV-31-1133-00-R100100 µlCHF 459.00
More Information
Product Details
Synonyms Actin, Aortic Smooth Muscle; alpha Smooth Muscle Actin; Alpha-actin-2; Cell Growth-inhibiting Gene 46 Protein
Product Type Recombinant Antibody
Properties
Clone RM253
Isotype Rabbit IgG
Source/Host Rabbit
Immunogen/Antigen A synthetic peptide corresponding to the N-terminus of human alpha smooth muscle Actin.
Application

Immunohistochemistry (IHC): 1:100-1:2500 dilution
Western Blot (WB): 1:1000-1:2000 dilution

Crossreactivity Human
Mouse
Specificity

This antibody reacts to human and mouse alpha smooth muscle Actin (alpha-Actin-2). This antibody may also react to bovine or rat alpha smooth muscle Actin, as predicted by immunogen homology.

Purity Protein A purified.
Purity Detail Protein A affinity purified from an animal origin-free culture supernatant.
Concentration N/A
Formulation Liquid. 50% Glycerol/PBS with 1% BSA and 0.09% sodium azide.
Isotype Negative Control

Rabbit IgG

Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

Accession Number P62736
Declaration Manufactured by RevMab Biosciences.
Shipping and Handling
Shipping BLUE ICE
Long Term Storage -20°C
Handling Advice Avoid freeze/thaw cycles.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF
Description

Actins are a family of globular multi-functional proteins that form microfilaments and are important for cell movement and the tensing (contraction) of muscles. ACTA2 (alpha smooth muscle actin; α-SMA) is one of 6 different actin isoforms and is involved in the contractile apparatus of smooth muscle. Smooth muscles line the internal organs, including the blood vessels, stomach, and intestines. Within smooth muscle cells, smooth muscle α-2 actin forms the core of structures called sarcomeres, which are necessary for muscles to contract. ACTA2 (as with all the actins) is extremely highly conserved and found in nearly all mammals. Mutations in this gene cause a variety of vascular diseases, such as thoracic aortic disease, coronary artery disease, stroke, Moyamoya disease and multisystemic smooth muscle dysfunction syndrome. ACTA2 is often used as a marker of myofibroblast formation.

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