RECQL2 抗体 (AA 1223-1432)
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- 抗原 See all RECQL2 (WRN) 抗体
- RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))
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抗原表位
- AA 1223-1432
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This RECQL2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- CQTNSVQTDL FSSTKPQEEQ KTSLVAKNKI CTLSQSMAIT YSLFQEKKMP LKSIAESRIL PLMTIGMHLS QAVKAGCPLD LERAGLTPEV QKIIADVIRN PPVNSDMSKI SLIRMLVPEN IDTYLIHMAI EILKHGPDSG LQPSCDVNKR RCFPGSEEIC SSSKRSKEEV GINTETSSAE RKRRLPVWFA KGSDTSKKLM DKTKRGGLFS
- 交叉反应
- 人
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1223-1432 of human WRN (NP_000544.2).
- 亚型
- IgG
- Top Product
- Discover our top product WRN Primary Antibody
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- 应用备注
- WB,1:200 - 1:1000
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 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.
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- 抗原
- RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))
- 别名
- WRN (WRN 产品)
- 别名
- RECQ3 antibody, RECQL2 antibody, RECQL3 antibody, xBLM antibody, recq2 antibody, recql2 antibody, recql3 antibody, AI846146 antibody, ffa-1 antibody, xwrn antibody, RGD1564788 antibody, Werner syndrome RecQ like helicase antibody, mediator of RNA polymerase II transcription subunit 34 antibody, Bloom syndrome RecQ like helicase antibody, Werner syndrome, RecQ helicase-like L homeolog antibody, WRN antibody, LOC9327212 antibody, blm antibody, Wrn antibody, wrn.L antibody
- 背景
- This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging.,WRN,RECQ3,RECQL2,RECQL3,Epigenetics & Nuclear Signaling,DNA Damage & Repair,Cell Biology & Developmental Biology,Apoptosis,WRN
- 分子量
- 162 kDa
- 基因ID
- 7486
- UniProt
- Q14191
- 途径
- DNA Damage Repair
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