MYO5A antibody (AA 1760-1840)
Quick Overview for MYO5A antibody (AA 1760-1840) (ABIN7222624)
Target
See all MYO5A AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 1760-1840
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Purpose
- Myosin VA Polyclonal Antibody
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Specificity
- Myosin VA Polyclonal Antibody detects endogenous levels of Myosin VA 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 C-terminal region of human Myosin VA at AA range: 1760-1840
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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), 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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- MYO5A (Myosin VA (MYO5A))
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Alternative Name
- Myosin VA
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Background
- Rabbit Anti-Myosin VA Polyclonal Antibody,MYO5A, MYH12, Unconventional myosin-Va, Dilute myosin heavy chain, non-muscle, Myosin heavy chain 12, Myosin-12, Myoxin,MYO5A is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by MYO5A is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.,Unconventional myosin-Va
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Molecular Weight
- observerd band 220kDa
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Gene ID
- 4644
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UniProt
- Q9Y4I1
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Pathways
- Hormone Transport, Peptide Hormone Metabolism
Target
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