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Catalog Number | orb345579 |
---|---|
Category | Antibodies |
Description | FIV matrix protein p15 antibody |
Species/Host | Rabbit |
Clonality | Polyclonal |
Tested applications | ELISA, IHC, WB |
Reactivity | Virus |
Isotype | IgG |
Immunogen | This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to amino acids from an internal region of FIV Matrix Protein p15. |
Concentration | 1.22 mg/mL |
Dilution range | ELISA: 1:5,000 - 1:20,000, IHC: User Optimized, WB: 1:1,000 - 1:10,000 |
Form/Appearance | Liquid (sterile filtered) |
Purity | This affinity purified antibody is directed against FIV Matrix Protein p15. The product was affinity purified from monospecific antiserum by immunoaffinity chromatography. |
Conjugation | Unconjugated |
UniProt ID | P16087 |
NCBI | 120815 |
Storage | Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. |
Buffer/Preservatives | 0.01% (w/v) Sodium Azide |
Alternative names | rabbit anti-Feline immunodeficiency virus matrix p Read more... |
Note | For research use only |
Application notes | This affinity purified antibody has been tested for use in ELISA and western blotting and suitable for immunocytochemistry. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 15 kDa in size corresponding to FIV Matrix Protein p15 by western blotting in the appropriate cell lysate or extract. |
Expiration Date | 12 months from date of receipt. |
Western blot using Biorbyt's affinity purified anti-FIV Matrix Protein p15 to detect p15 in the culture supernatant of FIV-infected feline CrFK cells (lane 2, arrowhead). Lane 1 is an uninfected control. Virions were enriched by ultracentrifugation, lysed, resolved by electrophoresis, and transferred to nitrocellulose. The membrane was probed with the primary antibody at a 1:10000 dilution.
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