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Recombinant GLN1 抗体 (AA 100-200)

The 兔 单克隆 anti-GLN1 antibody (Clone GLUL-12902R) (ABIN8093214) specifically detects GLN1 in WB 和 IHC. The antibody is reactive with 人 samples.
产品编号 ABIN8093214
发货至: 中国
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Quick Overview for Recombinant GLN1 抗体 (AA 100-200) (ABIN8093214)

抗原

See all GLN1 抗体
GLN1 (Glutamine Synthetase (GLN1))

抗体类型

Recombinant Antibody

适用

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人

宿主

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兔

克隆类型

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单克隆

标记

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This GLN1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)

质量等级

Carrier-free

克隆位点

GLUL-12902R
  • 抗原表位

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    AA 100-200

    原理

    Glutamine Synthetase Antibody / GLUL (azide and preservative free)

    免疫原

    A recombinant fragment (around amino acids 100-200) of human GLUL protein (exact sequence is proprietary) was used as the immunogen for the GLUL/Glutamine synthetase antibody.

    亚型

    IgG, kappa
  • 应用备注

    1. Optimal dilution of the GLUL/Glutamine synthetase antibody should be determined by the researcher.

    2. This GLUL/Glutamine synthetase antibody is recombinantly produced by expression in CHO cells.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C,-80 °C

    储存方法

    GLUL/Glutamine synthetase antibody with sodium azide - store at 2 to 8oC, antibody without sodium azide - store at -20 to -80oC.
  • 抗原

    GLN1 (Glutamine Synthetase (GLN1))

    别名

    Glutamine Synthetase

    背景

    Glutamate-ammonia ligase is a cytosolic enzyme encoded by the GLUL gene and commonly referred to as Glutamine synthetase. GLUL Antibody for WB GLUL/12902R is developed for western blot detection of this key metabolic enzyme in protein lysates. GLUL catalyzes the ATP-dependent conversion of glutamate and ammonia into glutamine and plays an essential role in nitrogen metabolism, neurotransmitter recycling, and cellular metabolic regulation.

    In western blot experiments, glutamine synthetase typically appears as a band near its predicted molecular weight of approximately 42 kDa on SDS-PAGE. Brain and liver lysates frequently produce strong immunoreactive signal because GLUL expression is enriched in astrocytes of the central nervous system and in pericentral hepatocytes within the liver. These tissues are therefore commonly used as positive controls in immunoblot workflows evaluating glutamine synthetase expression. Other tissues and cultured cell lines may show weaker bands depending on metabolic activity and cellular dependence on glutamine synthesis.

    Western blot analysis is particularly useful for evaluating relative GLUL protein levels across tissues or experimental treatments. Because glutamine synthetase is a soluble cytoplasmic enzyme, it is typically extracted efficiently using standard detergent-based lysis buffers such as RIPA or NP-40. After electrophoresis and membrane transfer, GLUL most often appears as a single predominant immunoreactive band corresponding to the full-length protein, allowing clear interpretation of immunoblot results. In some samples, minor band variation may occur due to protein turnover products or post-translational modifications, but the dominant species generally aligns with the expected molecular size.

    Immunoblot-based detection of GLUL is frequently used in studies examining metabolic regulation, hypoxia responses, and tumor-associated metabolic reprogramming. Altered glutamine synthetase expression has been described in hepatocellular carcinoma and other malignancies, where western blot analysis can help evaluate metabolic pathway activation and glutamine dependence. As a recombinant rabbit monoclonal reagent, GLUL Antibody for WB GLUL/12902R provides consistent target recognition suitable for immunoblot analysis of glutamine synthetase protein expression across diverse experimental systems.

    UniProt

    P15104

    途径

    Positive Regulation of Peptide Hormone Secretion
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