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Merck

F3165

モノクローナル抗FLAG® M2抗体 マウス宿主抗体

clone M2, purified immunoglobulin (Purified IgG1 subclass), buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)

ANTI-FLAG® M2 antibody, Mouse monoclonal

別名:

抗ddddk, 抗dykddddk

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サイズを選択してください

0.2 MG

¥41,680

1 MG

¥85,600

5 MG

¥211,500

¥41,680

単価¥52,100割引20%

本日発送予定詳細


バルクの問い合わせ

この商品について

NACRES:
NA.32
UNSPSC Code:
12352203

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製品名

モノクローナル抗FLAG® M2抗体 マウス宿主抗体, clone M2, purified immunoglobulin (Purified IgG1 subclass), buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)

biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin (Purified IgG1 subclass)

antibody product type

primary antibodies

clone

M2, monoclonal

form

buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)

purified by

using Protein A

species reactivity

all

concentration

3.8-4.2 mg/mL

technique(s)

western blot: 10 μg/mL (Protein A)

isotype

IgG1

immunogen sequence

DYKDDDDK

shipped in

dry ice

storage temp.

−20°C

Quality Level

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当該品目
F9291A9594A8592
clone

M2, monoclonal

clone

M2, monoclonal

clone

M2, monoclonal

clone

M2, monoclonal

conjugate

unconjugated

conjugate

biotin conjugate

conjugate

CY3 conjugate

conjugate

peroxidase conjugate

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

antibody form

purified immunoglobulin (Purified IgG1 subclass)

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

species reactivity

all

species reactivity

all

species reactivity

all

species reactivity

all

form

buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)

form

buffered aqueous glycerol solution

form

buffered aqueous solution (Supplied as a solution in 10 mM sodium phosphate)

form

buffered aqueous glycerol solution

Application

マウスで産生されるモノクローナル抗FLAG® M2抗体は以下で使用されています:
  • イムノブロッティング
  • 免疫沈降
  • 免疫細胞化学
  • 免疫蛍光法
  • ELISA
  • EIA
  • クロマチン免疫沈降
  • 電子顕微鏡法
  • フローサイトメトリー
  • スーパーシフトアッセイ

その他の用途を参照するには、メルクのFLAG®文献ポータルをご覧ください。

General description

抗Flag M2抗体は、Flag融合タンパク質の検出に使用されています。本モノクローナル抗体は、マウスで作成されており、N-末端、Met N-末端、およびC-末端のFLAG配列を認識します。本抗体はまた、内部のFLAGも認識できます。M2は、M1抗体とは異なり、カルシウム依存性ではありません。
F3165は、タンパク質A樹脂を用いてアフィニティー精製されるため、抗FLAG M2抗体だけでなく少量の自然マウスIgGを含み、ほとんどの用途で感度が改善されています。
精製方法 - タンパク質A

Immunogen

FLAG;ペプチド配列DYKDDDDK

Preparation Note

抗体溶液を、3%の無脂肪ミルクを含むトリス緩衝生理食塩水、pH 8.0で、0.5~10 μg/mLに希釈してください。
未希釈の抗体を、分注後–20℃で保管します。繰り返し凍結・解凍することは推奨しません。
注:時間とともに、分子内疎水性相互作用により少量の精製抗体が溶液から沈殿することがあります。本製品で沈殿が認められた場合、バイアルを短時間遠心分離し、沈殿をペレット化します。使用には、澄明な上清から必要量の抗体溶液を取り出します。これにより、ウエスタンブロットまたは免疫沈降アプリケーションにおける精製抗体の性能は変わりません。

Legal Information

ANTI-FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany

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保管分類

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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文書ライブラリにアクセスする

Casey C Fowler et al.
Nature communications, 10(1), 3684-3684 (2019-08-17)
Bacterial toxins with an AB5 architecture consist of an active (A) subunit inserted into a ring-like platform comprised of five delivery (B) subunits. Salmonella Typhi, the cause of typhoid fever, produces an unusual A2B5 toxin known as typhoid toxin. Here
Fangzhi Tan et al.
Nature communications, 10(1), 3733-3733 (2019-08-21)
Hearing loss is the most common sensory disorder. While gene therapy has emerged as a promising treatment of inherited diseases like hearing loss, it is dependent on the identification of gene delivery vectors. Adeno-associated virus (AAV) vector-mediated gene therapy has
Hong Zhu et al.
Molecular biology of the cell, 24(11), 1619-1637 (2013-04-12)
Charcot-Marie-Tooth (CMT) disease is an inherited neurological disorder. Mutations in the small integral membrane protein of the lysosome/late endosome (SIMPLE) account for the rare autosomal-dominant demyelination in CMT1C patients. Understanding the molecular basis of CMT1C pathogenesis is impeded, in part
T P Molitor et al.
Oncogenesis, 2, e48-e48 (2013-06-05)
The vaccinia-related kinases (VRKs) comprise a branch of the casein kinase family. VRK1, a ser/thr kinase with a nuclear localization, is the most well-studied paralog and has been described as a proproliferative protein. In lower eukaryotes, a loss of VRK1
Jeong Gu Kang et al.
Scientific reports, 9(1), 11960-11960 (2019-08-21)
Despite the increased interest in epigenetic research, its progress has been hampered by a lack of satisfactory tools to control epigenetic factors in specific genomic regions. Until now, many attempts to manipulate DNA methylation have been made using drugs but

資料

Comparison of elution techniques for small-scale protein purification of FLAG® tag proteins using anti-FLAG® M2 magnetic beads.

関連コンテンツ

Protein and nucleic acid interaction reagents and resources for investing protein-RNA, protein-DNA, and protein-protein interactions and associated applications.

タンパク質-RNA、タンパク質-DNA、タンパク質-タンパク質相互作用の検討および関連するアプリケーションのためのタンパク質-核酸相互作用試薬およびリソース。

EZviewTM Red Protein A and ANTI-FLAG® M2 Affinity Gels: Immunoprecipitation with Enhanced Visibility Affinity Beads - Technical Article - July 2001

質問

1–5/5 質問  
  1. Is there a recommended dilution for capture (sandwich) based ELISA?

    1 回答
    1. Monoclonal ANTI-FLAG® M2 may be used in EIA procedures. Typically, a fusion protein containing a FLAG® peptide sequence is directly adsorbed (or otherwise presented) within the wells of a multiwell polystyrene plate. The Monoclonal ANTI-FLAG® M2 antibody may be diluted up to 1:50,000 for subsequent incubation within the plate wells. Detection may be accomplished using Anti-Mouse IgG-Peroxidase (Cat. No. A9044) or equivalent, diluted 1:10,000, followed by an appropriate substrate for visualization.

      Dilutions for use as the capture antibody in an ELISA have not been evaluated. We would recommend that the end-user optimize the protocol following the recommendations found here:
      https://www.sigmaaldrich.com/technical-documents/protocol/protein-biology/elisa/elisa-procedures#antigen_coating

      役に立ちましたか?

  2. What is the recommended dilution for conducting western blotting using this antibody?

    1 回答
    1. The recommended dilution for Western Blot is 10 µg/mL. Please see the link below to review additional information, including protocols:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/274/912/f3165dat-ms.pdf

      役に立ちましたか?

  3. What is the recommended dilution for conducting immunoprecipitation (IP) using the M2 antibody?

    1 回答
    1. The general starting recommendation for conducting immunoprecipitation (IP) using the F3165, anti-FLAG M2 antibody, is 10 μg/mL.

      役に立ちましたか?

  4. What type of light chain is present on the FLAG M2 antibody?

    1 回答
    1. Test has not been conducted to determine whether the light chains of the antibody F3165, Monoclonal ANTI-FLAG® M2 antibody produced in mouse, are kappa or lambda. However, based on customer feedback, it appears that the M2 monoclonal antibody has lambda light chains and not kappa. A probe with anti-kappa did not yield a signal, while anti-lambda produced a good signal.

      役に立ちましたか?

  5. What is the difference between F1804 and F3165 product?

    1 回答
    1. Product F1804 and F3165 are both Monoclonal ANTI-FLAG M2 antibodies produced in mouse Clone M2, with the same starting material. The distinction between the products lies in their purification methods. F3165 is immunoglobulin purified, while F1804 is immunogen affinity purified. F1804, being more purified, is expected to exhibit reduced background and less non-specific staining compared to F3165. Both products are suitable for western blotting, immunofluorescence, and immunoprecipitation.

      役に立ちましたか?

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    星5/5個です。

    Great Anti Flag primary

    Works well for our western blot analysis of flag tagged recombinant proteins

    Googleで翻訳する

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