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FA2H 抗体

FA2H 适用: 人, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7257435
发货至: 中国
  • 抗原 See all FA2H 抗体
    FA2H (Fatty Acid 2-Hydroxylase (FA2H))
    适用
    • 33
    • 19
    • 12
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 大鼠
    宿主
    • 27
    • 6
    克隆类型
    • 29
    • 4
    多克隆
    标记
    • 16
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FA2H antibody is un-conjugated
    应用范围
    • 26
    • 15
    • 13
    • 2
    • 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 FA2H (NP_077282.3).
    亚型
    IgG
  • 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
    FA2H (Fatty Acid 2-Hydroxylase (FA2H))
    别名
    FA2H (FA2H 产品)
    别名
    FAAH antibody, FAH1 antibody, FAXDC1 antibody, SCS7 antibody, SPG35 antibody, RGD1310347 antibody, Wdr59 antibody, Faxdc1 antibody, G630055L08Rik antibody, MGC85470 antibody, MGC97767 antibody, cb1044 antibody, zgc:153777 antibody, fatty acid 2-hydroxylase antibody, fatty acid 2-hydroxylase L homeolog antibody, fatty acid hydroxylase antibody, FA2H antibody, Fa2h antibody, fa2h.L antibody, fa2h antibody, Tsp_11648 antibody, Ilyop_0703 antibody, Celly_1453 antibody, Weevi_1515 antibody, Fluta_1455 antibody, Mesop_3301 antibody
    背景
    This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.
    分子量

    Observed_MW: 38 kDa

    Calculated_MW: 18 kDa/42 kDa

    基因ID
    79152
    UniProt
    Q7L5A8
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