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PYGL 抗体 (AA 313-804) (Fluoro647)

The 兔 多克隆 anti-PYGL antibody is suitable to detect PYGL in samples from 人, 大鼠 和 小鼠. It has been validated for FACS.
产品编号 ABIN8022432
发货至: 中国
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Quick Overview for PYGL 抗体 (AA 313-804) (Fluoro647) (ABIN8022432)

抗原

See all PYGL 抗体
PYGL (phosphorylase, Glycogen, Liver (PYGL))

适用

  • 68
  • 33
  • 25
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 76
  • 2

克隆类型

  • 76
  • 2
多克隆

标记

  • 26
  • 12
  • 7
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PYGL antibody is conjugated to Fluoro647

应用范围

  • 36
  • 26
  • 16
  • 13
  • 13
  • 10
  • 10
  • 9
  • 8
  • 3
  • 3
  • 3
Flow Cytometry (FACS)
  • 抗原表位

    • 15
    • 12
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 313-804

    原理

    Anti-PYGL Antibody Fluoro647 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 PYGL recombinant protein (Position: K313-K804).

    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

    PYGL (phosphorylase, Glycogen, Liver (PYGL))

    别名

    PYGL

    背景

    Background: Glycogen phosphorylase, liver form (PYGL), also known as human liver glycogen phosphorylase (HLGP), is an enzyme that in humans is encoded by the PYGL gene on chromosome 14. This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Gene Full Name: glycogen phosphorylase L

    基因ID

    5836

    UniProt

    P06737

    途径

    Carbohydrate Homeostasis, Cellular Glucan Metabolic Process
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