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WNV M antibody (C-Term)

The Rabbit Polyclonal anti-WNV M antibody has been validated for ELISA. It is suitable to detect WNV M in samples from West Nile Virus (WNV).
Catalog No. ABIN6990506

Quick Overview for WNV M antibody (C-Term) (ABIN6990506)

Target

WNV M (West Nile Virus Matrix (WNV M))

Reactivity

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West Nile Virus (WNV)

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This WNV M antibody is un-conjugated

Application

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ELISA
  • Binding Specificity

    AA 220-270, C-Term

    Purification

    West Nile Virus Matrix Antibody is affinity chromatography purified via peptide column.

    Immunogen

    West Nile virus matrix antibody was raised against a synthetic peptide corresponding to 15 amino acids near the carboxy terminus of the West Nile virus matrix protein. The immunogen is located within amino acids 220 - 270 of West Nile Virus Matrix.

    Isotype

    IgG
  • Application Notes

    West Nile virus matrix antibody can be used for the detection of the West Nile virus matrix protein in ELISA. It will detect 10 ng of free peptide at 1 μ,g/mL.  

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    West Nile Virus Matrix Antibody is supplied in PBS containing 0.02 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C,4 °C

    Storage Comment

    West Nile Virus Matrix antibody can be stored at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    WNV M (West Nile Virus Matrix (WNV M))

    Alternative Name

    West Nile Virus Matrix

    Target Type

    Viral Protein

    Background

    West Nile Virus Matrix Antibody: West Nile Virus (WNV) is a member of the Flaviviridae, a plus-stranded virus family that includes St. Louis encephalitis virus, yellow fever virus, and Dengue virus. WNV was initially isolated in 1937 in the West Nile region of Uganda and has become prevalent in Africa, Asia, and Europe. It has rapidly spread across the United States with cases being observed in every continental state. Virus particles consist of a dense core made up of the core/capsid protein encapsulating the RNA genome surrounded by a membrane envelope embedded with envelope and matrix proteins. However, when the viruses are inside of infected cells, the matrix protein exists in its "pre-M" form as a heterodimer with the envelope proteins. Cleavage of the "pre-M" protein to its mature form occurs during release of the virus, this cleavage leas to the dissociation of the heterodimers. The WNV receptor has recently been identified as alpha v beta 3 integrin.

    Gene ID

    912267

    NCBI Accession

    NP_776012

    UniProt

    P06935
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