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Merck

S1265

Sigma-Aldrich

Anti-Sheep IgG (whole molecule) antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.46

biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

technique(s)

indirect ELISA: 1:50,000-1:100,000

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

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General description

Whole antiserum is fractionated and then further purified by ion exchange chromatography to provide the IgG fraction of antiserum. This fraction is essentially free of other rabbit serum proteins. Antiserum is determined to be immunospecific for sheep IgG by immunoelectrophoresis (IEP) versus sheep IgG and normal sheep serum. Identity and purity of the antibody is established by immunoelectrophoresis (IEP). Electrophoresis of the product followed by diffusion versus the anti-rabbit IgG and the anti-rabbit whole serum result in single arcs of precipitation in the γ region.

Specificity

Binds all sheep Igs

Immunogen

purified sheep IgG

Application

Anti-Sheep IgG (whole molecule) antibody produced in rabbit has been used in:
  • Enzyme-linked immunosorbent assay (ELISA)
  • Immunoprecipitation
  • labelling electrodes in immunosensor systems

Biochem/physiol Actions

Digestion of IgG by papain generates fragment antigen binding (Fab). Pepsin digestion of IgG results in fragment crystallisable (fc). IgG antibody has enormous therapeutic potential and the Fc is involved in the development of therapeutic antibody.

Physical form

Solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as preservative.

Disclaimer

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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Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Effect of diet composition on pregnancy outcome in overnourished rapidly growing adolescent sheep
Wallace JM, et al.
The British Journal of Nutrition, 96(6), 1060-1068 (2006)
Asli Devrekanli et al.
Journal of cell science, 125(Pt 22), 5453-5466 (2012-09-08)
The chitin synthase that makes the primary septum during cell division in budding yeasts is an important therapeutic target with an unknown activation mechanism. We previously found that the C2-domain of the Saccharomyces cerevisiae Inn1 protein plays an essential but
An electrochemical immunosensor for milk progesterone using a continuous flow system11Editors Selection
Pemberton RM et al.
Biosensors And Bioelectronics, 16(9), 715-723 (2001)
Frederick van Deursen et al.
The EMBO journal, 31(9), 2195-2206 (2012-03-22)
Mcm10 is essential for chromosome replication in eukaryotic cells and was previously thought to link the Mcm2-7 DNA helicase at replication forks to DNA polymerase alpha. Here, we show that yeast Mcm10 interacts preferentially with the fraction of the Mcm2-7
Cecile Evrin et al.
The EMBO journal, 37(19) (2018-08-15)
The eukaryotic replisome disassembles parental chromatin at DNA replication forks, but then plays a poorly understood role in the re-deposition of the displaced histone complexes onto nascent DNA. Here, we show that yeast DNA polymerase α contains a histone-binding motif

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