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Merck

IP50

Millipore

Protein G Immunoprecipitation Kit

sufficient for 50 assays

Synonim(y):

Immunoprecipitation kit

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About This Item

Kod UNSPSC:
12352203
NACRES:
NA.32

zastosowanie

sufficient for 50 assays

metody

immunoprecipitation (IP): suitable

temp. przechowywania

2-8°C

Zastosowanie

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.

Cechy i korzyści

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

Uwaga dotycząca przygotowania

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

Piktogramy

FlameExclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 3


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Patricia Workman et al.
Journal of bacteriology, 194(13), 3512-3521 (2012-05-01)
The BamA protein of Escherichia coli plays a central role in the assembly of β-barrel outer membrane proteins (OMPs). The C-terminal domain of BamA folds into an integral outer membrane β-barrel, and the N terminus forms a periplasmic polypeptide transport-associated
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
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
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
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

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