RNF8 antibody

别称:E3 ubiquitin-protein ligase RNF8 (hRNF8)|RING finger protein 8|RING-type E3 ubiquitin transferase RNF8|RNF8|KIAA0646 antibody
货号:FNab07362反应性:Human, Mouse, Rat
宿主:Rabbit验证实验:ELISA, WB, IHC, IF
克隆性:polyclonal亚型:IgG
规格 价格
100μg RMB ¥1900
50μg RMB ¥1140
货期: 三个工作日+顺丰快递时长
  • 产品介绍
  • 实验结果
  • 实验条件
  • 常见问题
产品名称
RNF8 antibody
货号
FNab07362
规格
100μg
状态
liquid
纯化方法
Immunogen affinity purified
纯度
≥95% as determined by SDS-PAGE
克隆性
polyclonal
亚型
IgG
存储
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
免疫原信息
免疫原
ring finger protein 8
别称
E3 ubiquitin-protein ligase RNF8 (hRNF8)|RING finger protein 8|RING-type E3 ubiquitin transferase RNF8|RNF8|KIAA0646 antibody
UniProt ID
O76064
分子量
56-60 kDa
验证实验
验证实验
ELISA, WB, IHC, IF
建议稀释比例
WB: 1:500-1:2000; IHC: 1:20-1:200; IF: 1:20-1:200
验证图片
HeLa cells were subjected to SDS PAGE followed by western blot with FNab07362(RNF8 Antibody) at dilution of 1:600
Immunohistochemistry of paraffin-embedded human testis tissue slide using FNab07362(RNF8 Antibody) at dilution of 1:50
背景介绍
E3 ubiquitin-protein ligase that plays a key role in DNA damage signaling via 2 distinct roles: by mediating the 'Lys-63'-linked ubiquitination of histones H2A and H2AX and promoting the recruitment of DNA repair proteins at double-strand breaks(DSBs) sites, and by catalyzing 'Lys-48'-linked ubiquitination to remove target proteins from DNA damage sites. Following DNA DSBs, it is recruited to the sites of damage by ATM-phosphorylated MDC1 and catalyzes the 'Lys-63'-linked ubiquitination of histones H2A and H2AX, thereby promoting the formation of TP53BP1 and BRCA1 ionizing radiation-induced foci(IRIF). Also controls the recruitment of UIMC1-BRCC3(RAP80-BRCC36) and PAXIP1/PTIP to DNA damage sites. Also recruited at DNA interstrand cross-links(ICLs) sites and catalyzes 'Lys-63'-linked ubiquitination of histones H2A and H2AX, leading to recruitment of FAAP20/C1orf86 and Fanconi anemia(FA) complex, followed by interstrand cross-link repair. H2A ubiquitination also mediates the ATM-dependent transcriptional silencing at regions flanking DSBs in cis, a mechanism to avoid collision between transcription and repair intermediates. Promotes the formation of 'Lys-63'-linked polyubiquitin chains via interactions with the specific ubiquitin-conjugating UBE2N/UBC13 and ubiquitinates non-histone substrates such as PCNA. Substrates that are polyubiquitinated at 'Lys-63' are usually not targeted for degradation. Also catalyzes the formation of 'Lys-48'-linked polyubiquitin chains via interaction with the ubiquitin-conjugating UBE2L6/UBCH8, leading to degradation of substrate proteins such as CHEK2, JMJD2A/KDM4A and KU80/XRCC5: it is still unclear how the preference toward 'Lys-48'-versus 'Lys-63'-linked ubiquitination is regulated but it could be due to RNF8 ability to interact with specific E2 specific ligases. For instance, interaction with phosphorylated HERC2 promotes the association between RNF8 and UBE2N/UBC13 and favors the specific formation of 'Lys-63'-linked ubiquitin chains. Promotes non-homologous end joining(NHEJ) by promoting the 'Lys-48'-linked ubiquitination and degradation the of KU80/XRCC5. Following DNA damage, mediates the ubiquitination and degradation of JMJD2A/KDM4A in collaboration with RNF168, leading to unmask H4K20me2 mark and promote the recruitment of TP53BP1 at DNA damage sites. In addition to its function in damage signaling, also plays a role in higher-order chromatin structure by mediating extensive chromatin decondensation. Involved in the activation of ATM by promoting histone H2B ubiquitination, which indirectly triggers histone H4 'Lys-16' acetylation(H4K16ac), establishing a chromatin environment that promotes efficient activation of ATM kinase. Required in the testis, where it plays a role in the replacement of histones during spermatogenesis. At uncapped telomeres, promotes the joining of deprotected chromosome ends by inducing H2A ubiquitination and TP53BP1 recruitment, suggesting that it may enhance cancer development by aggravating telomere-induced genome instability in case of telomeric crisis. Promotes the assembly of RAD51 at DNA DSBs in the absence of BRCA1 and TP53BP1 Also involved in class switch recombination in immune system, via its role in regulation of DSBs repair. May be required for proper exit from mitosis after spindle checkpoint activation and may regulate cytokinesis. May play a role in the regulation of RXRA-mediated transcriptional activity. Not involved in RXRA ubiquitination by UBE2E2.
抗体可以回收利用几次?

一般抗体不推荐回收利用,抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。

FineTest公司也做过一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定。

注:我们将孵育完毕后剩余的抗体回收到离心管中置于4℃保存,效价高的抗体可至少保存1周,重复利用3次左右。

FineTest公司抗体buffer成分是什么?

FineTest抗体成分一般是PBS含proclin300或sodium azide、BSA、50%甘油;也有一些是PBS含proclin300或sodium azide,50%甘油。防腐剂proclin300或sodium azide是常用的防腐剂,广泛应用于实验室和工业中。

FineTest公司抗体的保存温度和时间?

大部分抗体是放在-20℃保存,直标流式抗体需要放在2-8℃保存,质保期一年,质保期内抗体出现售后,可进行退货或换货。

一般抗体超过一年质保期仍旧可以使用,我们可以提供技术支持服务。

FineTest公司抗体使用需要稀释吗?用什么溶液稀释?

除了直标流式抗体为即用型,不用稀释。其他抗体一般为浓缩型,使用时需要按照说明书建议稀释比例稀释。

不同实验使用的稀释液不同,用PBST, TBST, 抗体封闭液等常用抗体稀释液均可。

免疫组化实验抗体的修复方式?

常用修复液:Tris-EDTA缓冲液(Tris-EDTA Buffer, pH 9.0);柠檬酸盐缓冲液(Citrate Buffer, pH 6.0)

热修复:

方法1:沸水浴修复,将盛有修复液和玻片的烧杯置于沸水浴环境,保持外部沸腾状态15min,自然冷却至室温;

方法2:微波修复,将盛有修复液和玻片的烧杯置于微波炉中,高火5min,停火3min,中火5min,自然冷却至室温。

如何选择二抗?

(1)二抗是和一抗反应的,所以二抗必须是抗一抗宿主物种,比如一抗来源于兔,对应二抗则选择抗兔二抗,比如羊抗兔或驴抗兔。

(2)根据实验类型选择二抗偶联物,比如做ELISA, 蛋白质印迹,IHC实验,常用酶联二抗,如HRP,AP等标记。而免疫荧光实验,流式细胞术实验中,则用荧光蛋白或染料标记,比如FITC,Cy3等。

产品对比