Actin antibody (AA 1-80)
Quick Overview for Actin antibody (AA 1-80) (ABIN7213464)
Target
See all Actin (ACTA1) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 1-80
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Purpose
- Actin α1 Polyclonal Antibody
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Specificity
- Actin α1 Polyclonal Antibody detects endogenous levels of Actin α1 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the N-terminal region of human Actin alpha1 at AA range: 1-80
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:20000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
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Alternative Name
- Actin alpha1
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Background
- Rabbit Anti-Actin α1 Polyclonal Antibody,ACTA1, ACTA, Actin, alpha skeletal muscle, Alpha-actin-1,Actin, alpha 1, skeletal muscle encoded by ACTA1 belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.,Actin alpha skeletal muscle
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Gene ID
- 58
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UniProt
- P68133
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Pathways
- Caspase Cascade in Apoptosis, Myometrial Relaxation and Contraction, Skeletal Muscle Fiber Development
Target
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