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Lipin 1 Protein (LPIN1) (Myc-DYKDDDDK Tag)

LPIN1 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2724880
发货至: 中国
  • 抗原 See all Lipin 1 (LPIN1) 蛋白
    Lipin 1 (LPIN1)
    蛋白类型
    Recombinant
    宿主
    • 3
    • 3
    • 2
    资源
    • 4
    • 2
    • 2
    HEK-293 Cells
    标记
    This Lipin 1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human LPIN1 / Lipin-1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product LPIN1 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    Lipin 1 (LPIN1)
    别名
    Lpin1,lipin-1 (LPIN1 产品)
    别名
    LPIN1 Protein, pap1 Protein, PAP1 Protein, 4631420P06 Protein, Kiaa0188 Protein, Lipin1 Protein, fld Protein, mKIAA0188 Protein, zgc:194552 Protein, zgc:194558 Protein, lipin1 Protein, lipin 1 Protein, phosphatidate phosphatase LPIN1 Protein, LPIN1 Protein, lpin1 Protein, LOC100539289 Protein, Lpin1 Protein
    背景
    This gene 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, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their full-length structures have not been determined.
    分子量
    98.5 kDa
    NCBI登录号
    NP_663731
    途径
    Monocarboxylic Acid Catabolic Process
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