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ACSL4 抗体 (AA 1-280)

This anti-ACSL4 antibody is a 兔 多克隆 antibody detecting ACSL4 in WB, IHC 和 IF. Suitable for 人. This Primary Antibody has been cited in 1 publication.
产品编号 ABIN6136458
发货至: 中国

Quick Overview for ACSL4 抗体 (AA 1-280) (ABIN6136458)

抗原

See all ACSL4 抗体
ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

适用

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宿主

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克隆类型

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多克隆

标记

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This ACSL4 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • 抗原表位

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    AA 1-280

    序列

    MAKRIKAKPT SDKPGSPYRS VTHFDSLAVI DIPGADTLDK LFDHAVSKFG KKDSLGTREI LSEENEMQPN GKVFKKLILG NYKWMNYLEV NRRVNNFGSG LTALGLKPKN TIAIFCETRA EWMIAAQTCF KYNFPLVTLY ATLGKEAVVH GLNESEASYL ITSVELLESK LKTALLDISC VKHIIYVDNK AINKAEYPEG FEIHSMQSVE ELGSNPENLG IPPSRPTPSD MAIVMYTSGS TGRPKGVMMH HSNLIAGMTG QCERIPGLGP KDTYIGYLPL

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-280 of human ACSL4 (NP_004449.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    说明

    HIGH QUALITY

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • Zhang, Wang, Cui, Deng, Xu, Yu, Cichello, Serrero, Ying, Liu: "Morphologically and Functionally Distinct Lipid Droplet Subpopulations." in: Scientific reports, Vol. 6, pp. 29539, (2018) (PubMed).

  • 抗原

    ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

    别名

    ACSL4

    背景

    The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants.,ACSL4,ACS4,FACL4,LACS4,MRX63,MRX68,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,ACSL4

    分子量

    74 kDa/79 kDa

    基因ID

    2182

    UniProt

    O60488
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