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HPGD 抗体

HPGD 适用: 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7234276
发货至: 中国
  • 抗原 See all HPGD 抗体
    HPGD (Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))
    适用
    • 40
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    小鼠
    宿主
    • 33
    • 5
    • 2
    克隆类型
    • 36
    • 4
    多克隆
    标记
    • 25
    • 3
    • 3
    • 3
    • 1
    • 1
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    This HPGD antibody is un-conjugated
    应用范围
    • 24
    • 16
    • 9
    • 7
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
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    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen Affinity Purification
    免疫原
    Recombinant Mouse 15-hydroxyprostaglandin dehydrogenase [NAD(+)] protein
    亚型
    IgG
    Top Product
    Discover our top product HPGD Primary Antibody
  • 应用备注
    IHC 1:100-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.69 mg/mL
    缓冲液
    PBS with 0.05 % Proclin300 and 50 % glycerol, pH 7.4.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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
    HPGD (Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))
    别名
    HPGD (HPGD 产品)
    别名
    CBR antibody, SDR21C1 antibody, hCBR1 antibody, 15-PGDH antibody, PGDH antibody, PGDH1 antibody, PHOAR1 antibody, SDR36C1 antibody, MGC80546 antibody, MGC79454 antibody, AV026552 antibody, carbonyl reductase 1 antibody, 15-hydroxyprostaglandin dehydrogenase antibody, hydroxyprostaglandin dehydrogenase 15-(NAD) antibody, 15-hydroxyprostaglandin dehydrogenase L homeolog antibody, hydroxyprostaglandin dehydrogenase 15 (NAD) antibody, CBR1 antibody, HPGD antibody, hpgd.L antibody, hpgd antibody, pgdh antibody, Hpgd antibody, PTRG_03214 antibody, VDBG_09957 antibody
    背景
    This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene.
    UniProt
    Q8VCC1
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