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M4812

Sigma-Aldrich

Anti-Myosin Va (LF-18) antibody produced in rabbit

enhanced validation

~0.4 mg/mL, affinity isolated antibody, buffered aqueous solution

Synonyme(s) :

Anti-GS1, Anti-MYH12, Anti-MYO5, Anti-MYR12

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Conjugué

unconjugated

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

primary antibodies

Clone

polyclonal

Forme

buffered aqueous solution

Poids mol.

antigen 190 kDa

Espèces réactives

chicken, rat

Validation améliorée

independent
Learn more about Antibody Enhanced Validation

Concentration

~0.4 mg/mL

Technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:200 using rat and chicken cerebellum sections
microarray: suitable
western blot: 1:1,000 using a rat brain extract

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... MYO5A(4644)
mouse ... Myo5a(17918)
rat ... Myo5a(25017)

Description générale

Anti-myosin Va (LF-18) recognizes myosin Va (190kDa). Myosin 5a is encoded by the gene mapped to human chromosome 15q21.2. The encoded protein is a member of the unconventional myosin family. It is a two-headed motor containing two identical heavy chains and multiple light chains. Myosin Va is widely expressed, but at high levels in the brain, testes and melanocytes.

Immunogène

synthetic peptide located near the C-terminus of chicken myosin Va (amino acids 1782-1799 with N-terminally added lysine) conjugated to KLH. This sequence is identical in human, mouse and rat.

Application

Anti-Myosin Va (LF-18) antibody produced in rabbit has been used in:
  • Western blot.
  • In situ proximity ligation assay (PLA).
  • Glutathione S-transferase (GST)-spinophilin co-sedimentation assay.

Actions biochimiques/physiologiques

Myosin 5a is an actin-based molecular motor responsible for transport of secretory granules in various cell systems, including insulin granule. Additionally, it also mediates the transport of cargo such as cell-surface receptors, pigment and organelles like endoplasmic reticulum to the plasma membrane. The encoded protein facilitates pigmentation and synaptic activity in the central nervous system. Genetic variations in the gene are associated with the development of immunological and neurological diseases, including Griscelli syndrome type 1 and Elejalde syndrome.

Forme physique

Solution in 0.01 M phosphate buffered saline containing 1% BSA and 15 mM sodium azide.

Stockage et stabilité

For continuous use, store at 2-8°C for up to one month. For prolonged storage, freeze in working aliquots at -20°C. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Autres remarques

In order to obtain best results in different techniques and preparations we recommend determining optimal working dilutions by titration test.

Clause de non-responsabilité

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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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Ianina L Conte et al.
Journal of cell science, 129(3), 592-603 (2015-12-18)
Weibel-Palade body (WPB)-actin interactions are essential for the trafficking and secretion of von Willebrand factor; however, the molecular basis for this interaction remains poorly defined. Myosin Va (MyoVa or MYO5A) is recruited to WPBs by a Rab27A-MyRIP complex and is
Genome-Wide Meta-Analysis of Sciatica in Finnish Population
Lemmela S, et al.
PLoS ONE, 11 (2016)
The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L
Assis LH, et al.
Scientific Reports (2017)
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene.
Pastural E, et al.
Nature Genetics, 16, 289-292 (1997)
Josephine A Carew et al.
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society, 33(10), e14162-e14162 (2021-05-04)
The motor protein, Myosin 5a (Myo5a) is known to play a role in inhibitory neurotransmission in gastric fundus. However, there is no information regarding the relative expression of total Myo5a, or of its alternative exon splice variants, across the stomach.

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