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PTH 抗体 (AA 1-115)

This anti-PTH antibody is a 小鼠 单克隆 antibody detecting PTH in ELISA. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN1724741
发货至: 中国

Quick Overview for PTH 抗体 (AA 1-115) (ABIN1724741)

抗原

See all PTH 抗体
PTH (Parathyroid Hormone (PTH))

适用

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宿主

  • 124
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  • 4
小鼠

克隆类型

  • 130
  • 112
单克隆

标记

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  • 1
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This PTH antibody is un-conjugated

应用范围

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ELISA

克隆位点

2C7
  • 抗原表位

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    • 9
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-115

    原理

    PTH Antibody

    纯化方法

    Ascitic fluid

    免疫原

    Purified recombinant fragment of human PTH(aa1-115) expressed in E. Coli.

    亚型

    IgG2b
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Ascitic fluid containing 0.03 % 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

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Sprague, Evenepoel, Curzi, González, Husserl, Kopyt, Sterling, Mix, Wong: "Simultaneous control of PTH and CaxP Is sustained over three years of treatment with cinacalcet HCl." in: Clinical journal of the American Society of Nephrology : CJASN, Vol. 4, Issue 9, pp. 1465-76, (2009) (PubMed).

    Koshizuka, Ogata, Shiraki, Hosoi, Seichi, Takeshita, Nakamura, Kawaguchi: "Distinct association of gene polymorphisms of estrogen receptor and vitamin D receptor with lumbar spondylosis in post-menopausal women." in: European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, Vol. 15, Issue 10, pp. 1521-8, (2006) (PubMed).

  • 抗原

    PTH (Parathyroid Hormone (PTH))

    别名

    PTH

    物质类

    Hormone

    背景

    The protein encoded by this gene is a hormone secreted by parathyroid cells. This hormone elevates blood Ca2+ level by dissolving the salts in bone and preventing their renal excretion. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH).

    分子量

    12.9 kDa

    基因ID

    5741

    UniProt

    P01270

    途径

    cAMP Metabolic Process, Regulation of Carbohydrate Metabolic Process
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