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WBSCR22 抗体 (AA 1-281)

WBSCR22 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6150175
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
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-281
    适用
    • 29
    • 10
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    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
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    序列
    MASRGRRPEH GGPPELFYDE TEARKYVRNS RMIDIQTRMA GRALELLYLP ENKPCYLLDI GCGTGLSGSY LSDEGHYWVG LDISPAMLDE AVDREIEGDL LLGDMGQGIP FKPGTFDGCI SISAVQWLCN ANKKSENPAK RLYCFFASLF SVLVRGSRAV LQLYPENSEQ LELITTQATK AGFSGGMVVD YPNSAKAKKF YLCLFSGPST FIPEGLSENQ DEVEPRESVF TNERFPLRMS RRGMVRKSRA WVLEKKERHR RQGREVRPDT QYTGRKRKPR F
    交叉反应
    人, 大鼠
    产品特性
    Polyclonal Antibodies
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-281 of human WBSCR22 (NP_059998.2).
    亚型
    IgG
    Top Product
    Discover our top product WBSCR22 Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000,IF,1:50 - 1:100
    限制
    仅限研究用
  • 状态
    Liquid
    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)
    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.,BUD23,HASJ4442,HUSSY-3,MERM1,PP3381,WBMT,WBSCR22,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,WBSCR22
    分子量
    24 kDa/31 kDa/33 kDa
    基因ID
    114049
    UniProt
    O43709
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