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Magna ChIP® Kulki magnetyczne z białkiem A+G

provides a rapid, reproducible and efficient collection of immunocomplexes for ChIP and RIP assays

Synonim(y):

Kulki magnetyczne ChIP, Kulki magnetyczne ChIP A+G, Kulki magnetyczne ChIP A/G

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Gabaryty przesyłkiSKUDostępnośćCena netto
50 reactions

Dostępne do wysyłki DZISIAJzKuehne + Nagel Sp. z o.o.

1420,00 zł

Informacje o tej pozycji

NACRES:
NA.84
UNSPSC Code:
41105501

1420,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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Quality Level

packaging

pkg of 1 mL

manufacturer/tradename

Magna ChIP®

storage condition

do not freeze

particle size

~3 μm

shipped in

wet ice

storage temp.

2-8°C

General description

Chromatin immunoprecipitation (ChIP) has been widely adapted for the study of gene-specific and genome-wide distribution of specific DNA and RNA-binding proteins or protein modifications. Similar to standard protein immunoprecipitation assays, ChIP involves isolation of immunocomplexes using a solid medium, such as agarose or magnetic beads, coupled to either IgG binding recombinant protein A or protein G. Experiments comparing protein A vs. protein G vs. protein A/G magnetic bead blends revealed that a mixture of protein A and G beads worked well with a wide variety of antibody isotypes. The use of Protein A/G bead blends eliminated the need to consider which beads or kit to use in order match a particular antibody/bead binding affinity combination. In addition to simplifying the procedure, comparing the use of either protein A or protein G alone, protein A/G magnetic bead blends improved signal-to-noise ratios without decreasing the recovery of input chromatin in ChIP assays.

Application

This blend of protein A+G magnetic beads allows for the use of a wider range of antibodies than A or G alone & provides a rapid, reproducible & efficient collection of immunocomplexes for chromatin immunoprecipitations (ChIP) and RNA immunoprecipitations (RIP) assays.

Use 20 µL of bead suspension per ChIP application. Includes sufficient reagents for 50 precipitation reactions. Disperse beads thoroughly before pipetting by rapid vortex.

Used to detect/quantify: Protein A+G

Physical form

Liquid suspension. Supplied as magnetic bead slurry in phosphate buffered saline, pH 7.4, containing 0.01% Tween®-20 and 0.09% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of shipment. Do Not Freeze.

Analysis Note

Routinely evaluated by Chromatin immunoprecipitation (ChIP) using HeLa nuclear extracts and the Magna ChIP® A Kit (Cat. #17-610).

Legal Information

MAGNA CHIP is a registered trademark of Merck KGaA, Darmstadt, Germany
TWEEN is a registered trademark of Croda International PLC

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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Ta pozycja
16-66116-66217-10085
shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

dry ice

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage condition

do not freeze

storage condition

do not freeze

storage condition

-

storage condition

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

packaging

pkg of 1 mL

packaging

pkg of 1 mL

packaging

pkg of 1 mL

packaging

-

particle size

~3 μm

particle size

~3 μm

particle size

~3 μm

particle size

-


Klasa składowania

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_c

Not applicable



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Powiązane treści

Chromatin immunoprecipitation (ChIP) has been widely adapted for the study of gene-specific and genome-wide distribution of specific DNA- and RNA-binding proteins or protein modifications. Similar to standard protein immunoprecipitation assays, ChIP involves isolation of immunocomplexes using a solid medium, such as agarose or magnetic beads, coupled to either IgG binding recombinant protein A or protein G. In a typical ChIP experiment either protein A or G is selected for enrichment depending on the antibody isotype. However, proteins A and G possess differing affinities for human and mouse IgGs. Complicating this choice, for some antibody isotypes there is affinity for both protein A and G. In addition, we have observed that independent of the isotype the affinity of a specific antibody for protein A or G can vary depending on the specific clone, purification method, and source.

Chromatin-immunoprecipitation (ChIP) followed by next generation sequencing (ChIP-seq) of the immunoprecipitated DNA is a powerful tool for the investigation of protein:DNA interactions. To perform ChIP-seq, chromatin is isolated from cells or tissues (with or without chemical crosslinking) and fragmented. Antibodies recognizing chromatinassociated proteins of interest are used to enrich the sample for specific chromatin fragments. The DNA is recovered, sequenced on various NGS platforms, and aligned to a reference genome to determine specific protein binding loci. ChIP-seq studies have increased our knowledge of transcription factor biology, DNA methylation and histone modifications.

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SKUNUMER GTIN
16-66304053252421549
16-663X04053252483646

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