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HSD17B4 抗体

HSD17B4 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7241504
发货至: 中国
  • 抗原 See all HSD17B4 抗体
    HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
    适用
    • 42
    • 22
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    • 1
    人, 小鼠, 大鼠
    宿主
    • 54
    • 3
    克隆类型
    • 54
    • 3
    多克隆
    标记
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    This HSD17B4 antibody is un-conjugated
    应用范围
    • 49
    • 21
    • 20
    • 15
    • 13
    • 13
    • 5
    • 5
    • 3
    • 2
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    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human HSD17B4
    亚型
    IgG
    Top Product
    Discover our top product HSD17B4 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
    0.3 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
    别名
    HSD17B4 (HSD17B4 产品)
    别名
    zgc:55545 antibody, zgc:77300 antibody, CG3415 antibody, DmMFE-2 antibody, Dmel\\CG3415 antibody, MFE-2 antibody, DBP antibody, MPF-2 antibody, PRLTS1 antibody, SDR8C1 antibody, 17-beta-HSD antibody, 17[b]-HSD antibody, 4 antibody, MFP2 antibody, Mfp-2 antibody, perMFE-2 antibody, hydroxysteroid (17-beta) dehydrogenase 4 antibody, hydroxysteroid 17-beta dehydrogenase 4 antibody, peroxisomal Multifunctional enzyme type 2 antibody, hsd17b4 antibody, HSD17B4 antibody, Mfe2 antibody, Hsd17b4 antibody
    背景
    The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8.
    分子量
    80 kDa
    UniProt
    P51659
    途径
    Monocarboxylic Acid Catabolic Process
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