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Merck

F6304

Sigma-Aldrich

抗FOXP2抗体 ウサギ宿主抗体

IgG fraction of antiserum, buffered aqueous solution

別名:

抗CAGH44抗体, 抗SPCH1抗体, 抗TNRC10抗体

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About This Item

MDL番号:
UNSPSCコード:
12352203
NACRES:
NA.41

由来生物

rabbit

結合体

unconjugated

抗体製品の状態

IgG fraction of antiserum

抗体製品タイプ

primary antibodies

クローン

polyclonal

形状

buffered aqueous solution

分子量

antigen ~80 kDa

化学種の反応性

human, mouse, rat

テクニック

microarray: suitable
western blot: 1:500-1:1,000 using extracts of Jurkat cells
western blot: 1:500-1:1,000 using mouse heart tissue extract

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

unmodified

遺伝子情報

human ... FOXP2(93986)
mouse ... Foxp2(114142)

詳細

The superfamily of Forkhead transcription factors (FOX) consists of more than 100 members, with orthologues expressed in a variety of species ranging from yeast to man. They are characterized by a common Forkhead (or winged helix) domain, a variant of the helix-turnhelix motif. Forkhead box P2 (FOXP2) transcripts encode for three different isoforms, I, II and III encoding for proteins of 715, 740, and 623 amino acids respectively. FOXP2 has a polyglutamine tract. FOXP1, FOXP2 and FOXP4 contain a complex N-terminal region responsible for transcriptional repression. This region contains various protein-protein interaction motifs conserved in all three proteins, including a zinc finger and a putative leucine zipper.

免疫原

synthetic peptide corresponding to amino acids 36-53 of human FOXP2, conjugated to KLH via a C-terminal lysine residue. The immunizing sequence is conserved in mouse and rat.

アプリケーション

Anti-FOXP2 antibody is suitable for:
  • western blot analysis as primary antibody of the embryonic cortex to study the expression of FoxP2 in neural precursors of the embryonic cortex.
  • immunohistochemistry of prostate gland cells to determine the expression level of FOXP2 in prostate cancer.
  • microarray
  • western blot at a dilution of 1:500-1:1,000 using extracts of Jurkat cells and mouse heart tissue extract.

生物化学的/生理学的作用

Forkhead box P2 (FOXP2) is the first gene relevant to the human ability to develop language, offering an opportunity to study neural mechanisms from a molecular perspective. Missense and nonsense mutations have been identifying in families with language impairment. Thus, a point mutation led to the isolation to FOXP2, whereas more recently a truncation was discovered in a family with speech and language difficulties as well.
Forkhead transcription factors (FOX) family consists of more than 100 members. It is widely expressed in a variety of species ranging from yeast to man. It has a common Forkhead (or Winged Helix) domain, a variant of the helix-turnhelix motif. It plays a key regulatory role in embryonic development, differentiation, apoptosis and tumorigenesis. Its subfamily P (FOXP1, FOXP2, FOXP3 and FOXP4) has well defined clinical implications in tumor suppression as well as autoimmunity and development. FOXP2 is composed of a polyglutamine tract and a complex N-terminal region responsible for transcriptional repression. The N-terminal region contains various protein-protein interaction motifs including a zinc finger and a putative leucine zipper. It has been reported that FOXP2 acts as a major part of a multiprotein complex that regulates diverse aspects of tissue restricted gene expression during development.

物理的形状

Solution in 0.01 M phosphate buffered saline, pH 7.4, and 15 mM sodium azide.

免責事項

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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保管分類コード

10 - Combustible liquids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

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


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

F6304-200UL:
F6304-BULK:
F6304-VAR:


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
MacDermot KD, et al.
American Journal of Human Genetics, 76(6), 1074-1074 (2005)
Ogyi Park et al.
Annals of the New York Academy of Sciences, 1051, 218-228 (2005-08-30)
Crohn's disease (CD) is a chronic inflammatory bowel disease typified by transmural inflammation affecting any part of the gastrointestinal tract. CD4(+)CD25(+) regulatory T cells (T(reg) cells) play important roles in intestinal homeostasis. Adoptive transfer of regulatory T cells into mice
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
Lai CSL, et al.
Brain, 126(Pt), 11-11 (2003)
David Tsui et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(1), 244-258 (2013-01-04)
The transcription factor FoxP2 has been associated with the development of human speech but the underlying cellular function of FoxP2 is still unclear. Here we provide evidence that FoxP2 regulates genesis of some intermediate progenitors and neurons in the mammalian
A forkhead-domain gene is mutated in a severe speech and language disorder.
Lai CS
Nature, 413(6855), 519-523 (2001)

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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