Anti-Actin antibody [AC-40] (ab92833)
- Product nameAnti-Actin antibody [AC-40]See all Actin primary antibodies ...
- DescriptionMouse monoclonal [AC-40] to Actin
- Tested applicationsWB, IHC-Fr more details
- Species reactivityReacts with: Mouse, Rat, Chicken, Human
Predicted to work with: a wide range of other species
Synthetic peptide corresponding to Actin (C terminal). Attached to a Multiple Antigen Peptide (MAP) backbone.
- Storage instructionsStore at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
- Storage bufferPreservative: 0.02% Sodium azide
Constituents: 0.2% BSA, 1.2% Sodium acetate
- Concentration information loading...
- PurityImmunogen affinity purified
- Clonality Monoclonal
- Clone numberAC-40
Our Abpromise guarantee covers the use of ab92833 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||WB: Use a concentration of 2 µg/ml. Predicted molecular weight: 42 kDa.|
|IHC-Fr||IHC-Fr: Use a concentration of 4 µg/ml.|
- FunctionActins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
- Involvement in diseaseDefects in ACTA1 are the cause of nemaline myopathy type 3 (NEM3) [MIM:161800]. A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-or rod-like structures in muscle fibers on histologic examination. The phenotype at histological level is variable. Some patients present areas devoid of oxidative activity containg (cores) within myofibers. Core lesions are unstructured and poorly circumscribed.
Defects in ACTA1 are a cause of myopathy congenital with excess of thin myofilaments (MPCETM) [MIM:161800]. A congenital muscular disorder characterized at histological level by areas of sarcoplasm devoid of normal myofibrils and mitochondria, and replaced with dense masses of thin filaments. Central cores, rods, ragged red fibers, and necrosis are absent.
Defects in ACTA1 are a cause of congenital myopathy with fiber-type disproportion (CFTD) [MIM:255310]; also known as congenital fiber-type disproportion myopathy (CFTDM). CFTD is a genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However, these findings are not specific and can be found in many different myopathic and neuropathic conditions.
- Sequence similaritiesBelongs to the actin family.
- Cellular localizationCytoplasm > cytoskeleton.
- ACTA antibody
- ACTA1 antibody
- Actin alpha skeletal muscle antibody
- Actin antibody
- actin, alpha 1, skeletal muscle 1 antibody
- actin, alpha 1, skeletal muscle antibody
- Actin, alpha skeletal muscle antibody
- actina antibody
- actine antibody
- ACTS_HUMAN antibody
- aktin antibody
- Alpha Actin 1 antibody
- Alpha skeletal muscle Actin antibody
- alpha skeletal muscle antibody
- alpha-actin antibody
- Alpha-actin-1 antibody
- ASMA antibody
- CFTD antibody
- CFTD1 antibody
- CFTDM antibody
- MPFD antibody
- NEM1 antibody
- NEM2 antibody
- NEM3 antibody
- nemaline myopathy type 3 antibody
References for Anti-Actin antibody [AC-40] (ab92833)
ab92833 has not yet been referenced specifically in any publications.