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HSD17B13 抗体

HSD17B13 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7011012
发货至: 中国
  • 抗原 See all HSD17B13 抗体
    HSD17B13 (Hydroxysteroid (17-Beta) Dehydrogenase 13 (HSD17B13))
    适用
    • 33
    • 29
    • 23
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    人, 大鼠, 小鼠
    宿主
    • 47
    • 1
    克隆类型
    • 47
    • 1
    多克隆
    标记
    • 11
    • 4
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    • 2
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    • 2
    • 2
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    • 2
    • 1
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    This HSD17B13 antibody is un-conjugated
    应用范围
    • 35
    • 15
    • 14
    • 13
    • 13
    • 6
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human HSD17B13 (NP_835236.2).
    亚型
    IgG
    Top Product
    Discover our top product HSD17B13 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 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
    HSD17B13 (Hydroxysteroid (17-Beta) Dehydrogenase 13 (HSD17B13))
    别名
    HSD17B13 (HSD17B13 产品)
    别名
    NIIL497 antibody, SCDR9 antibody, SDR16C3 antibody, AI047820 antibody, PAN1B-like antibody, Pan1b antibody, hydroxysteroid 17-beta dehydrogenase 13 antibody, hydroxysteroid (17-beta) dehydrogenase 13 antibody, HSD17B13 antibody, Hsd17b13 antibody
    背景
    Hydroxysteroid (17-beta) dehydrogenase 13, also designated Short-chain dehydrogenase/reductase 9 (SCDR9), which regulate the availability of steroids within various tissues throughout the body. HSD17B13 is a 300 amino acid secreted protein that is highly expressed in liver and is also detected in ovary, bone marrow, kidney, brain, lung, skeletal muscle, bladder and testis. The gene encoding HSD17B13 maps to chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
    分子量

    Observed_MW: 33 kDa

    Calculated_MW: 29 kDa/33 kDa

    基因ID
    345275
    UniProt
    Q7Z5P4
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