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WBSCR22 抗体

WBSCR22 适用: 人, 大鼠 IF, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263325
发货至: 中国
  • 抗原 See all WBSCR22 抗体
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    适用
    • 35
    • 10
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 大鼠
    宿主
    • 31
    • 4
    克隆类型
    • 33
    • 2
    多克隆
    标记
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WBSCR22 antibody is un-conjugated
    应用范围
    • 28
    • 14
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human WBSCR22 (NP_059998.2).
    亚型
    IgG
    Top Product
    Discover our top product WBSCR22 Primary Antibody
  • 应用备注
    IHC 1:50-1:200 IF 1:50-1:100
    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
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    别名
    WBSCR22 (WBSCR22 产品)
    别名
    MGC82375 antibody, wbmt antibody, pp3381 antibody, hussy-3 antibody, hasj4442 antibody, zgc:162306 antibody, HASJ4442 antibody, HUSSY-3 antibody, MERM1 antibody, PP3381 antibody, WBMT antibody, 1110003N24Rik antibody, Williams-Beuren syndrome chromosome region 22 antibody, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog antibody, BUD23, rRNA methyltransferase and ribosome maturation factor antibody, williams Beuren syndrome chromosome region 22 antibody, hypothetical protein antibody, WBSCR22 antibody, bud23.L antibody, bud23 antibody, CpipJ_CPIJ001394 antibody, PAAG_00857 antibody, MCYG_07273 antibody, PGTG_07527 antibody, PGTG_12505 antibody, BUD23 antibody, Bud23 antibody
    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.
    基因ID
    114049
    UniProt
    O43709
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