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ABHD11 抗体 (Middle Region)

ABHD11 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5516392
发货至: 中国
  • 抗原 See all ABHD11 抗体
    ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))
    抗原表位
    • 8
    • 7
    • 7
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    • 30
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 33
    • 2
    克隆类型
    • 35
    多克隆
    标记
    • 14
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ABHD11 antibody is un-conjugated
    应用范围
    • 23
    • 21
    • 12
    • 2
    • 1
    • 1
    Western Blotting (WB)
    序列
    QQTGRRVLTV DARNHGDSPH SPDMSYEIMS QDLQDLLPQL GLVPCVVVGH
    纯化方法
    Affinity purified
    免疫原
    The immunogen is a synthetic peptide directed towards the middle region of human ABHD11
    Top Product
    Discover our top product ABHD11 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原
    ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))
    别名
    ABHD11 (ABHD11 产品)
    别名
    Abhd11l1 antibody, Wbscr21 antibody, wbscr21 antibody, Wbscr21l antibody, pp1226 antibody, WBSCR21 antibody, 1110054D16Rik antibody, A630008N09Rik antibody, abhydrolase domain containing 11 antibody, abhydrolase domain containing 11 L homeolog antibody, Abhd11 antibody, ABHD11 antibody, abhd11 antibody, LOC732867 antibody, abhd11.L antibody
    背景
    This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been described, but their biological validity has not been determined.

    Alias Symbols: PP1226, WBSCR21,

    Protein Size: 315
    基因ID
    83451
    NCBI登录号
    NM_001145364, NP_001138836
    UniProt
    Q8NFV4
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