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GBA 抗体 (C-Term)

GBA 适用: 人 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1107380
发货至: 中国
  • 抗原 See all GBA 抗体
    GBA (Glucosidase, Beta, Acid (GBA))
    抗原表位
    • 7
    • 5
    • 5
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    C-Term
    适用
    • 53
    • 29
    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 64
    • 10
    克隆类型
    • 57
    • 17
    多克隆
    标记
    • 33
    • 15
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    This GBA antibody is un-conjugated
    应用范围
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    序列
    EGSQRVGLVA SQKNDLDAVA LMHPDGSAVV VVLNRSSKDV PLTIKDPAVG
    交叉反应 (详细)
    Species reactivity (expected):Bovine, Rat, Dog, PigSpecies reactivity (tested):Human
    纯化方法
    Purified using peptide immunoaffinity column
    免疫原
    Synthetic peptide directed towards the C-term region of human Glucosylceramidase
    Top Product
    Discover our top product GBA Primary Antibody
  • 限制
    仅限研究用
  • 溶解方式
    Add 50 μL of distilled water to a final concentration of 1 mg/mL.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
  • 抗原
    GBA (Glucosidase, Beta, Acid (GBA))
    别名
    Glucosylceramidase (GBA 产品)
    别名
    GBA1 antibody, GCB antibody, GLUC antibody, BETA-GLUCOSIDASE antibody, T12J13.8 antibody, T12J13_8 antibody, beta glucosidase 25 antibody, PSPTO3318 antibody, PSPTO4290 antibody, GC antibody, GCase antibody, betaGC antibody, glucosylceramidase beta antibody, beta glucosidase 25 antibody, beta-glucosidase antibody, Beta-glucosidase antibody, glucosidase, beta, acid antibody, glucosylceramidase antibody, bglX-2 antibody, GBA antibody, BGLU25 antibody, PSPTO_3318 antibody, bglX antibody, bglA4 antibody, Gba antibody, LOC100399524 antibody, bglA.2 antibody, bglX-2 antibody
    背景
    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.Synonyms: Acid beta-glucosidase, Alglucerase, Beta-glucocerebrosidase, D-glucosyl-N-acylsphingosine glucohydrolase, GBA, GC, GLUC, Imiglucerase
    基因ID
    2629
    NCBI登录号
    NM_000157
    途径
    Cellular Glucan Metabolic Process
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