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Merck
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安全性情報

HPA005552

Sigma-Aldrich

抗ACSL4抗体 ウサギ宿主抗体

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

別名:

抗LACS4抗体 ウサギ宿主抗体, 抗長鎖アシル-CoAシンセターゼ4抗体 ウサギ宿主抗体, 抗長鎖脂肪酸-CoAリガーゼ4抗体 ウサギ宿主抗体

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About This Item

UNSPSCコード:
12352203
Human Protein Atlas Number:
NACRES:
NA.43
結合体:
unconjugated
application:
IHC
クローン:
polyclonal
化学種の反応性:
human
citations:
7
テクニック:
immunoblotting: 0.04-0.4 μg/mL
immunohistochemistry: 1:50-1:200

由来生物

rabbit

品質水準

結合体

unconjugated

抗体製品の状態

affinity isolated antibody

抗体製品タイプ

primary antibodies

クローン

polyclonal

製品種目

Prestige Antibodies® Powered by Atlas Antibodies

フォーム

buffered aqueous glycerol solution

化学種の反応性

human

テクニック

immunoblotting: 0.04-0.4 μg/mL
immunohistochemistry: 1:50-1:200

免疫原配列

MNYLEVNRRVNNFGSGLTALGLKPKNTIAIFCETRAEWMIAAQTCFKYNFPLVTLYATLGKEAVVHGLNESEASYLITSVELLESKLKTALLDISCVKHIIYVDNKAINKAEYPEGFEIHSMQSVEELGSNPENLGIPPSRPTPSDMAIV

UniProtアクセッション番号

輸送温度

wet 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 ... ACSL4(2182)

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関連するカテゴリー

詳細

ACSL4 (acyl-CoA synthetase long-chain family member 4) belongs to the family of mammalian long chain acyl-CoA synthetases. This family consists of five isoforms, one being ACSL4. It is localized to the endoplasmic reticulum (ER) associated with mitochondria, and peroxisome. It is expressed in smooth muscle and neuronal cells. However, its predominant expression is in steroidogenic tissues. It is highly expressed in spleen, placenta, testis, ovary, brain and adrenal cortex. ACSL4 gene is localized to human chromosome Xq23. The encoded protein has a molecular weight of 75kDa.

免疫原

長鎖脂肪酸-CoAリガ-ゼ4のPrEST (protein epitope signature tag)抗原リコンビナントタンパク質。

アプリケーション

Prestige抗体®は、Human Proteome Resource(HPR)プロジェクト(www.proteinatlas.org)によって開発・実証されたAtlas抗体です。抗体はすべて、数百の正常組織・疾病組織に対する免疫組織染色試験を行っています。これらの染色画像はHuman Protein Atlas(HPA)サイトで[Image Gallery]リンクをクリックするとご覧いただけます。さらに、ほとんどのPrestige抗体はプロテインアレイおよびウェスタンブロッティングの試験を行っています。試験のプロトコールおよびPrestige抗体、HPAに関する情報はsigma.com/prestigeをご覧ください。

生物化学的/生理学的作用

ACSL4 (acyl-CoA synthetase long-chain family member 4) has a higher affinity for arachidonic acid (AA) and eicosapentanoic acid (EPA), as opposed to other isoforms. Thus, it plays an essential role in AA metabolism. It is responsible for the de novo synthesis of diacylglycerol (DAG). ACSL4 also mediates the storage of fatty acids in the form of triacylglycerol. Two point mutations in this gene are linked with nonspecific mental retardation. ACSL4 expression is up-regulated in liver, colon and aggressive forms of breast cancer. It has potential as a marker for aggressive phenotype of breast cancer. This gene is linked to metabolic syndrome, as a mutation in ACSL4 gene leads to abnormal fatty acid composition of phosphatidylcholines present in plasma membrane. Inactivation of this gene is found in elliptocytosis, Alport syndrome, and mental retardation. Therefore, it is suggested that FACL4 regulates intellectual capability and coordination skills, through FACL4-derived arachidonoyl phospholipids.

特徴および利点

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

関連事項

Corresponding Antigen APREST74278

物理的形状

PBS溶液 (pH 7.2, 40%グリセロ-ルおよび0.02%アジ化ナトリウム含有)。

法的情報

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

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 1

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

HPA005552-25UL:
HPA005552-100UL:


最新バージョンのいずれかを選択してください:

試験成績書(COA)

Lot/Batch Number

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特定のバージョンが必要な場合は、ロット番号またはバッチ番号で特定の証明書を検索できます。

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

Lydie Cheval et al.
Function (Oxford, England), 5(4) (2024-07-10)
A detailed knowledge of the lipid composition of components of nephrons is crucial for understanding physiological processes and the development of kidney diseases. However, the lipidomic composition of kidney tubular segments is unknown. We manually isolated the proximal convoluted tubule
Xinyu Wu et al.
PloS one, 8(10), e77060-e77060 (2013-10-25)
The purpose of this study was to determine the role of long-chain fatty acyl-CoA synthetase 4 (ACSL4) in breast cancer. Public databases were utilized to analyze the relationship between ACSL4 mRNA expression and the presence of steroid hormone and human
Ilaria Meloni et al.
Nature genetics, 30(4), 436-440 (2002-03-13)
X-linked mental retardation (XLMR) is an inherited condition that causes failure to develop cognitive abilities, owing to mutations in a gene on the X chromosome. The latest XLMR update lists up to 136 conditions leading to 'syndromic', or 'specific', mental
Y Cao et al.
FEBS letters, 467(2-3), 263-267 (2000-02-17)
Fatty acid utilization is initiated by fatty acid-CoA ligase, which converts free fatty acids into fatty acyl-CoA esters. We have cloned previously the human long-chain fatty acid-CoA ligase 4 (FACL4), which is a central enzyme in controlling the free arachidonic
Miroslav Zeman et al.
The Tohoku journal of experimental medicine, 217(4), 287-293 (2009-04-07)
The composition of polyunsaturated fatty acids (PUFAs) in cell membranes and body tissues is altered in metabolic syndrome (MetS) and depressive disorder (DD). Within the cell, fatty acid coenzyme A (CoA) ligases (FACLs) activate PUFAs by esterifying with CoA. The

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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