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Lipin 1 抗体

The 兔 多克隆 anti-Lipin 1 antibody (ABIN7229428) specifically detects Lipin 1 in WB 和 ELISA. The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN7229428
发货至: 中国
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Quick Overview for Lipin 1 抗体 (ABIN7229428)

抗原

See all Lipin 1 (LPIN1) 抗体
Lipin 1 (LPIN1)

适用

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人, 小鼠

宿主

  • 85
  • 8
  • 3

克隆类型

  • 68
  • 28
多克隆

标记

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This Lipin 1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 原理

    Rabbit Anti-LPIN1 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of LPIN1 protein

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from part region of human LPIN1 protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

    储存液

    ProClin

    注意事项

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

    储存条件

    -20 °C

    储存方法

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    Lipin 1 (LPIN1)

    别名

    LPIN1

    背景

    Phosphatidate phosphatase LPIN1, Lipin-1LPIN1 encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, acute recurrent rhabdomyolysis, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes.

    分子量

    97kD

    基因ID

    23175

    UniProt

    Q14693

    途径

    Monocarboxylic Acid Catabolic Process
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