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Key Documents

M4812

Sigma-Aldrich

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

enhanced validation

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

同義詞:

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

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rabbit

共軛

unconjugated

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

buffered aqueous solution

分子量

antigen 190 kDa

物種活性

chicken, rat

加強驗證

independent
Learn more about Antibody Enhanced Validation

濃度

~0.4 mg/mL

技術

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

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

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

一般說明

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.

免疫原

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.

應用

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.

生化/生理作用

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.

外觀

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

儲存和穩定性

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.

其他說明

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

免責聲明

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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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L
Assis LH, et al.
Scientific Reports (2017)
Roles for myosin Va in RNA transport and turnover.
McCaffrey MW and Lindsay AJ.
Biochemical Society Transactions, 40, 1416-1420 (2012)
Myosin Va is required for normal photoreceptor synaptic activity
Libby RT, et al.
Journal of Cell Science, 117, 4509-4515 (2004)
Identification and validation of novel spinophilin-associated proteins in rodent striatum using an enhanced ex vivo shotgun proteomics approach.
Baucum AJ 2nd, et al.
Molecular and Cellular Proteomics, 9, 1243-1259 (2010)
Genome-Wide Meta-Analysis of Sciatica in Finnish Population
Lemmela S, et al.
PLoS ONE, 11 (2016)

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