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PKLR 抗体

PKLR 适用: 人 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7259945
发货至: 中国
  • 抗原 See all PKLR 抗体
    PKLR (Pyruvate Kinase, Liver and RBC (PKLR))
    适用
    • 69
    • 30
    • 20
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 66
    • 10
    克隆类型
    • 68
    • 8
    多克隆
    标记
    • 35
    • 8
    • 7
    • 6
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This PKLR antibody is un-conjugated
    应用范围
    • 51
    • 39
    • 36
    • 6
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human PKLR (NP_000289.1).
    亚型
    IgG
    Top Product
    Discover our top product PKLR Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    PKLR (Pyruvate Kinase, Liver and RBC (PKLR))
    别名
    PKLR (PKLR 产品)
    别名
    PK1 antibody, PKL antibody, PKR antibody, PKRL antibody, RPK antibody, Pklg antibody, wu:fd15e01 antibody, wu:fi37e08 antibody, pk1 antibody, PKLR antibody, Pk-1 antibody, Pk1 antibody, R-PK antibody, pklr antibody, pyruvate kinase L/R antibody, pyruvate kinase, liver and RBC antibody, pyruvate kinase, liver and RBC L homeolog antibody, pyruvate kinase liver and red blood cell antibody, pyruvate kinase PKLR-like antibody, PKLR antibody, Pklr antibody, pklr antibody, pklr.L antibody, LOC100621940 antibody
    背景
    The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene.
    基因ID
    5313
    UniProt
    P30613
    途径
    Ribonucleoside Biosynthetic Process
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