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ACSL4 抗体 (AA 36-237) (Fluoro550)

The Fluoro550-conjugated 兔 多克隆 anti-ACSL4 antibody (ABIN7966158) specifically detects ACSL4 in FACS. The antibody is reactive with 人, 大鼠 和 小鼠 samples.
产品编号 ABIN7966158
发货至: 中国
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Quick Overview for ACSL4 抗体 (AA 36-237) (Fluoro550) (ABIN7966158)

抗原

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

适用

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人, 大鼠, 小鼠

宿主

  • 99
  • 15
  • 1

克隆类型

  • 86
  • 29
多克隆

标记

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This ACSL4 antibody is conjugated to Fluoro550

应用范围

  • 81
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Flow Cytometry (FACS)
  • 抗原表位

    • 29
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    AA 36-237

    原理

    Anti-FACL4/ACSL4 Antibody Fluoro550 Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human FACL4/ACSL4 recombinant protein (Position: A36-E237).

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

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

    别名

    ACSL4

    背景

    Background: Long-chain-fatty-acid-CoA ligase 4 is an enzyme that in humans is encoded by the ACSL4 gene. It is mapped to Xq23. 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 cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants.

    Gene Full Name: acyl-CoA synthetase long chain family member 4

    基因ID

    2182

    UniProt

    O60488
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