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ERCC5 抗体 (N-Term)

This anti-ERCC5 antibody is a 兔 多克隆 antibody detecting ERCC5 in WB. Suitable for 人, 小鼠, 大鼠, Cow, 犬, 马, 兔 和 豚鼠.
产品编号 ABIN2785634
发货至: 中国

Quick Overview for ERCC5 抗体 (N-Term) (ABIN2785634)

抗原

See all ERCC5 抗体
ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

适用

  • 43
  • 12
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  • 2
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人, 小鼠, 大鼠, Cow, 犬, 马, 兔, 豚鼠

宿主

  • 38
  • 5

克隆类型

  • 39
  • 4
多克隆

标记

  • 31
  • 2
  • 1
  • 1
  • 1
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This ERCC5 antibody is un-conjugated

应用范围

  • 32
  • 16
  • 10
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  • 5
  • 5
  • 2
  • 1
  • 1
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Western Blotting (WB)
  • 抗原表位

    • 8
    • 5
    • 3
    • 3
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    N-Term

    序列

    NPQAIDIESE DFSSLPPEVK HEILTDMKEF TKRRRTLFEA MPEESDDFSQ

    预测反应

    Cow: 86%, Dog: 86%, Guinea Pig: 93%, Horse: 86%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%

    产品特性

    This is a rabbit polyclonal antibody against ERCC5. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the N terminal region of human ERCC5
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 1186 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

    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

    别名

    ERCC5

    背景

    Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    Alias Symbols: COFS3, ERCM2, UVDR, XPG, XPGC
    Protein Interaction Partner: UBC, CDK7, GTF2H1, POLR2A, EWSR1, ERCC6, SUMO2, PIDD1, BCL6, TAF10, ERCC3, NTHL1, GTF2H4, PCNA, ERCC2,
    Protein Size: 1186

    分子量

    133 kDa

    基因ID

    2073

    NCBI登录号

    NM_000123, NP_000114

    UniProt

    P28715

    途径

    DNA Damage Repair
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