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MAB880-A

Sigma-Aldrich

Anti-HIV Antibody, p24, clone 7A8.1

clone 7A8.1, Chemicon®, from mouse

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100 μG
CHF 278.00

CHF 278.00


Spedizione prevista il16 aprile 2025


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Cambia visualizzazione
100 μG
CHF 278.00

About This Item

Codice UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

CHF 278.00


Spedizione prevista il16 aprile 2025


Richiedi un ordine bulk

Origine biologica

mouse

Livello qualitativo

Forma dell’anticorpo

purified antibody

Tipo di anticorpo

primary antibodies

Clone

7A8.1, monoclonal

Reattività contro le specie

human

Produttore/marchio commerciale

Chemicon®

tecniche

immunocytochemistry: suitable
western blot: suitable

Isotipo

IgG1

Condizioni di spedizione

wet ice

Informazioni sul gene

human ... TARBP1(6894)

Specificità

Core protein p24. No cross-reactivity observed to other HIV proteins.

Immunogeno

Epitope: p24
p24 isolated from human (native) HIV infected cells.

Applicazioni

Anti-HIV Antibody, p24, clone 7A8.1 is an antibody against HIV for use in IC & WB.
Research Category
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral
Western Blot (1:100) or Immunoperoxidase or Immunofluorescence on human tissue (1:100).

Antibodies are not neutralizing. For extensive dilution, protein containing or other stabilizing medium should be used. Final working dilutions must be determined by end user.

Linkage

Replaces: MAB882

Stato fisico

Format: Purified
Purified. Supplied in 0.05M Tris Cl, pH 8.0.

Stoccaggio e stabilità

Maintain at 4°C in undiluted aliquots for up to 12 months.

Altre note

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Note legali

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Esclusione di responsabilità

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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Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Rui Liu et al.
The Journal of infectious diseases, 208(8), 1221-1230 (2013-07-16)
Many chronic human immunodeficiency virus (HIV) patients suffer from gastric complaints, including gastric tuberculosis and coinfection of other pathogens. Recent work has demonstrated that a variety of nonimmune cells can act as viral reservoirs, even at the early stage of
Shilpi Sharma et al.
Journal of virology, 93(11) (2019-03-15)
The cellular protein bone marrow stromal antigen-2 (BST-2)/tetherin acts against a variety of enveloped viruses by restricting their release from the plasma membrane. The HIV-1 accessory protein Vpu counteracts BST-2 by downregulating it from the cell surface and displacing it
Envelope proteins of spleen necrosis virus form infectious human immunodeficiency virus type 1 pseudotype vector particles, but fail to incorporate upon substitution of the cytoplasmic domain with that of Gibbon ape leukemia virus.
Stitz, J; Wolfrum, N; Buchholz, CJ; Cichutek, K
The Journal of General Virology null
Stosh Ozog et al.
Molecular therapy. Methods & clinical development, 13, 27-39 (2019-01-04)
Lentiviral vectors (LVs) pseudotyped with the measles virus hemagglutinin (H) and fusion (F) glycoproteins have been reported to more efficiently transduce hematopoietic stem and progenitor cells (HSPCs) compared with vesicular stomatitis virus glycoprotein (VSV-G) pseudotyped LVs. However, a limit to
Anje Sporbert et al.
PloS one, 8(5), e64023-e64023 (2013-05-24)
This study describes a simple technique that improves a recently developed 3D sub-diffraction imaging method based on three-photon absorption of commercially available quantum dots. The method combines imaging of biological samples via tri-exciton generation in quantum dots with deconvolution and

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