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Merck

A7827

Sigma-Aldrich

Alkaline Phosphatase-Anti-Alkaline Phosphatase antibody produced in mouse

clone AP1B9, purified immunoglobulin, buffered aqueous solution

Synonym(e):

APAAP

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About This Item

UNSPSC-Code:
12352203
NACRES:
NA.46

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

AP1B9, monoclonal

Beschreibung

Concentrate

Form

buffered aqueous solution

Methode(n)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:40 using human tonsil

Isotyp

IgG1

Versandbedingung

wet ice

Lagertemp.

2-8°C

Posttranslationale Modifikation Target

unmodified

Allgemeine Beschreibung

A soluble complex of calf intestinal alkaline phosphatase and mouse monoclonal antibodies to alkaline phosphatase. The product is a soluble complex of calf intestinal alkaline phosphatase and mouse monoclonal antibodies to alkaline phosphatase.
Monoclonal Anti-Alkaline Phosphatase (mouse IgG1 isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse.

Anwendung

Alkaline Phosphatase-Anti-Alkaline Phosphatase antibody produced in mouse has been used in:
  • Immunohistological analysis
  • Immunohistochemistry assay
  • Immunocytochemical staining

Apoptosis of β-cells in mouse pancreatic sections was analyzed by incubating section with TUNEL and anti-insulin antibody. APAAP was used as the secondary antibody and BCIP/NBT (Sigma) as the substrate.

Biochem./physiol. Wirkung

Mouse Monoclonal Alkaline Phosphatase Anti-Alkaline Phosphatase is a soluble complex formed from levamisole-resistant calf intestinal alkaline phosphatase and purified mouse monoclonal antibody to alkaline phosphatase. The use of a mouse monoclonal alkaline phosphatase anti-alkaline phosphatase (APAAP) complex, in conjunction with a primary mouse antibody and a secondary bridging antibody (anti-mouse IgG), results in an intense signal with a very low background, while avoiding problems inherent to the covalent conjugation of antibodies. The technology of unlabelled antibody peroxidase-anti peroxidase (PAP) and the alkaline phosphatase anti- alkaline phosphatase (APAAP) method has applications in immunostaining. APAAP monoclonal antibodies complex are homogenous and this method is effective and its sensitive.

Physikalische Form

Solution in 0.05 M Tris buffered saline, pH 8.0, containing 1 mM MgCl2, 1% bovine serum albumin and 15 mM sodium azide.

Haftungsausschluss

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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Lagerklassenschlüssel

10 - Combustible liquids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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J L Klein et al.
Bone marrow transplantation, 28(11), 1023-1029 (2002-01-10)
Fifty women with breast cancer metastatic to bone or bone marrow involvement on light microscopy at the time of initial evaluation were treated with high-dose chemotherapy (HDC) and peripheral blood progenitor cell (PBPC) transplantation with CD34(+) cell selection using the
APAAP complex: production and usage in immunocytochemical and immunohistochemical staining
Naseri M, et al.
Human Antibodies, 16(3-4), 107-115 (2007)
High-dose chemotherapy and CD34-selected peripheral blood progenitor cell transplantation for patients with breast cancer metastatic to bone and/or bone marrow
Klein JL, et al.
Bone Marrow Transplantation, 28(11), 1023-1023 (2001)
Tumor control in a model of bone marrow transplantation and acute liver-infiltrating B-cell lymphoma: an unpredicted novel function of cytomegalovirus
Erlach KC, et al.
Journal of Virology, 76(6), 2857-2870 (2002)
The onset of p53-dependent apoptosis plays a role in terminal differentiation of human normoblasts
Peller S, et al.
Oncogene, 22(30), 4648-4648 (2003)

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