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AB137644

Anti-KIAA1530抗体- N-terminal

Anti-KIAA1530 antibody - N-terminal

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(1 Publication)

Rabbit Polyclonal KIAA1530 antibody. Suitable for WB, ICC/IF and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human UVSSA aa 1-200.

查看别名

KIAA1530, UVSSA, UV-stimulated scaffold protein A

1 Images
Immunocytochemistry/ Immunofluorescence - Anti-KIAA1530 antibody - N-terminal (AB137644)
  • ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-KIAA1530 antibody - N-terminal (AB137644)

Immunofluorescence analysis of paraformaldehyde fixed A431 cells, labelling KIAA1530 with ab137644 at 1/200 dilution (left), costained with Hoechst 33342 (right).

关键信息

宿主种属

Rabbit

克隆

Polyclonal

亚型

IgG

不含载体蛋白

No

反应种属

Human

应用

ICC/IF, WB

applications

免疫原

Recombinant Fragment Protein within Human UVSSA aa 1-200. The exact immunogen used to generate this antibody is proprietary information.

Q2YD98

反应性数据

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "ICCIF" : {"fullname" : "Immunocytochemistry/ Immunofluorescence", "shortname":"ICC/IF"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/500 - 1/3000", "WB-species-notes": "<p></p>", "ICCIF-species-checked": "testedAndGuaranteed", "ICCIF-species-dilution-info": "1/100 - 1/1000", "ICCIF-species-notes": "<p></p>" } } }

性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Immunogen
存储溶液
pH: 7 Preservative: 0.01% Thimerosal (merthiolate) Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
运输条件
Blue Ice
推荐的短期储存条件
+4°C
推荐的长期储存条件
-20°C
分装信息
Upon delivery aliquot
储存信息
Avoid freeze / thaw cycle

产品实验方案

For this product, it's our understanding that no specific protocols are required. You can visit:

靶点信息

Factor involved in transcription-coupled nucleotide excision repair (TC-NER), a mechanism that rapidly removes RNA polymerase II-blocking lesions from the transcribed strand of active genes (PubMed : 22466610, PubMed : 22466611, PubMed : 22466612, PubMed : 32142649, PubMed : 32355176, PubMed : 34526721, PubMed : 38316879, PubMed : 38600235, PubMed : 38600236). Acts as a key adapter that promotes recruitment of factors involved in TC-NER (PubMed : 22466611, PubMed : 22466612, PubMed : 32142649, PubMed : 32355176, PubMed : 34526721, PubMed : 38600235, PubMed : 38600236). Facilitates the ubiquitination of the elongating form of RNA polymerase II (RNA pol IIo) at DNA damage sites, thereby promoting RNA pol IIo backtracking and access by the TC-NER machinery to lesion sites (PubMed : 22466611, PubMed : 32142649). Also promotes stabilization of ERCC6/CSB by recruiting deubiquitinating enzyme USP7 to TC-NER complexes, preventing UV-induced degradation of ERCC6 by the proteasome (PubMed : 22466611, PubMed : 22466612). Mediates the recruitment of the TFIIH complex and other factors that are required for nucleotide excision repair to RNA polymerase II (PubMed : 32142649, PubMed : 32355176, PubMed : 34526721, PubMed : 38600235, PubMed : 38600236). Also required to inactivate stalled RNA polymerase II by blocking the access of TCEA1/TFIIS, thereby preventing reactivation of RNA polymerase II (PubMed : 38316879). Not involved in processing oxidative damage (PubMed : 22466612).
See full target information UVSSA

文献 (1)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in pharmacology 13:777612 PubMed35295342

2022

The SKA3-DUSP2 Axis Promotes Gastric Cancer Tumorigenesis and Epithelial-Mesenchymal Transition by Activating the MAPK/ERK Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Chao Zhang,Shutao Zhao,Yuen Tan,Siwei Pan,Wen An,Qingchuan Chen,Xudong Wang,Huimian Xu
View all publications

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