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Merck

IP50

Protein G Immunoprecipitation Kit

sufficient for 50 assays

Sinônimo(s):

Immunoprecipitation kit

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1 KIT

R$ 4.190,00

R$ 4.190,00


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Sobre este item

NACRES:
NA.32
UNSPSC Code:
12352203

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usage

sufficient for 50 assays

Quality Level

technique(s)

immunoprecipitation (IP): suitable

storage temp.

2-8°C

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Este Item
AA0100ET0300IP0010
technique(s)

immunoprecipitation (IP): suitable

technique(s)

-

technique(s)

-

technique(s)

immunoprecipitation (IP): suitable

usage

sufficient for 50 assays

usage

sufficient for 100 assays

usage

sufficient for 100 assays

usage

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

Application

The kit is designed to allow maximal recovery of immunoprecipitates. It provides all the necessary reagents to perform immunoprecipitation from cell extracts of any protein to which a suitable antibody is available. Based on protein G, the kit binds to most commonly used antibodies. In addition, spin columns are provided to enable quick washes without the loss of protein G resin and thus protein yield is maximized.

Features and Benefits

  • Minimal loss of antigen-antibody bound beads during washing.
  • Minimal or no non-specific signals by increasing the stringency of the washing step.

Preparation Note

When preparing reagents, use ultrapure water (17M -cm)

Componentes do kit também disponíveis separadamente

Nº do produto
Descrição
SDS

  • S65465 M Sodium chloride solution 15 mLSDS

  • P3296Protein G Agarose 2 mLSDS

  • 7173610% Sodium dodecyl sulfate solution 1 mLSDS

related product

pictograms

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Classe de armazenamento

3 - Flammable liquids

wgk

WGK 3


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Hubert Arokium et al.
The Journal of biological chemistry, 282(48), 35104-35112 (2007-10-04)
During apoptosis, the pro-apoptotic protein Bax relocalizes from the cytosol to the mitochondrial outer membrane. This relocalization is associated to major conformational changes, namely at the N- and C-terminal ends of the protein. Substitution of residues located at critical positions
F Gautier et al.
Molecular and cellular biology, 31(4), 832-844 (2010-12-22)
Bcl-2 homologues (such as Bcl-x(L)) promote survival in part through sequestration of "activator" BH3-only proteins (such as Puma), preventing them from directly activating Bax. It is thus assumed that inhibition of interactions between activators and Bcl-x(L) is a prerequisite for
R Meller et al.
Cell death and differentiation, 10(5), 539-547 (2003-05-03)
Seizure-induced neuronal death may involve engagement of the BCL-2 family of apoptosis-regulating proteins. In the present study we examined the activation of proapoptotic BAD in cultured hippocampal neurons following seizures induced by removal of chronic glutamatergic transmission blockade. Kynurenic acid
Peter J Eastmond
The Plant cell, 19(4), 1376-1387 (2007-04-24)
Hydrogen peroxide is a major by-product of peroxisomal metabolism and has the potential to cause critical oxidative damage. In all eukaryotes, catalase is thought to be instrumental in removing this H(2)O(2). However, plants also contain a peroxisomal membrane-associated ascorbate-dependent electron
Phu Vuong et al.
Journal of bacteriology, 190(5), 1507-1517 (2008-01-01)
In Escherichia coli, YaeT, together with four lipoproteins, YfgL, YfiO, NlpB, and SmpA, forms a complex that is essential for beta-barrel outer membrane protein biogenesis. Data suggest that YfgL and YfiO make direct but independent physical contacts with YaeT. Whereas

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SKUGTIN
IP50-1KT04061833866092

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