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WBSCR22 抗体 (C-Term)

WBSCR22 适用: 人, 大鼠, 小鼠, 犬, Cow, 豚鼠, 马, Pig, 兔 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2789228
发货至: 中国
  • 抗原 See all WBSCR22 抗体
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    抗原表位
    • 9
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term
    适用
    人, 大鼠, 小鼠, 犬, Cow, 豚鼠, 马, Pig, 兔
    宿主
    • 25
    • 4
    克隆类型
    • 27
    • 2
    多克隆
    标记
    • 17
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WBSCR22 antibody is un-conjugated
    应用范围
    • 21
    • 9
    • 8
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    序列
    GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP
    预测反应
    Cow: 77%, Dog: 86%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 86%, Pig: 86%, Rabbit: 93%, Rat: 86%
    产品特性
    This is a rabbit polyclonal antibody against WBSCR22. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    Top Product
    Discover our top product WBSCR22 Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 298 AA

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    Lot specific
    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.
    注意事项
    Avoid repeated freeze-thaw cycles.
    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
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    别名
    WBSCR22 (WBSCR22 产品)
    背景
    This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. 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 found.
    Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
    Protein Interaction Partner: VCP, UBC, PKN1, OAS1, ZMYM3, THOC2, WDR74, REM1, PHLPP1, PPIP5K1, CUL3, SUMO2,
    Protein Size: 298
    分子量
    32 kDa
    基因ID
    114049
    NCBI登录号
    NM_001202560, NP_001189489
    UniProt
    C9K060
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