생물학적 소스
rabbit
Quality Level
항체 형태
serum
항체 생산 유형
primary antibodies
클론
polyclonal
종 반응성
mouse, human
종 반응성(상동성에 의해 예측)
primate (based on 100% sequence homology)
기술
ChIP: suitable (ChIP-seq)
western blot: suitable
NCBI 수납 번호
UniProt 수납 번호
배송 상태
dry ice
타겟 번역 후 변형
unmodified
유전자 정보
human ... RBPJ(3516)
관련 카테고리
일반 설명
Recombining binding protein suppressor of hairless (UniProt: Q06330; also known as CBF-1, Immunoglobulin kappa J region recombination signal binding protein 1, J kappa-recombination signal-binding protein, RBP-J, RBP-JK, RBP-J kappa, Renal carcinoma antigen NY-REN-30) is encoded by the RBPJ (also known as AOS3, CBF1, IGKJRB, IGKJRB1, KBF2, RBPJK, RBPSUH, SUH) gene (Gene ID: 3516) in human. RBP-J is a transcriptional regulator that plays a key role in Notch signaling. Acts as a transcriptional repressor when it is not associated with Notch proteins. It associates with several transcriptional co-repressors in the absence of Notch intracellular domain (NICD). Upon activation, following cleavage by gamma-secretase, NICD translocates to the nucleus and forms a transcriptional activation complex with RBPJ. This complex in turn recruits other co-activators and complex components, leading to regulated target gene expression. Genome-wide ChIP-seq profiling reveals both overlapping and non-overlapping chromatin-binding sites occupied by RBPJ and Notch1. Murine RBPJ-only sites are shown to be highly enriched for imputed REST (a DNA-binding transcriptional repressor) sites, whereas human RPBJ-only sites lack REST motifs and are more enriched for imputed CREB sites. Dysregulated RBPJ-dependent gene expression is seen in B-cell tumors associated with Epstein-Barr virus (EBV) and a majority of T-lymphoblastic leukemia/lymphoma (TLL) tumors having somatic Notch1 gain-of-function mutations.
특이성
This rabbit polyclonal antibody recognizes Recombining binding protein suppressor of hairless (RBP-J) in human and murine cells. It targets and epitope within the first 48 amino acids in the N-terminal region.
면역원
Epitope: N-terminus
GST-tagged recombinant fragment corresponding to the first 48 amino acids of human Recombining binding protein suppressor of hairless (RBP-J).
애플리케이션
Anti-RBPJ, Cat. No. ABE384, is a highly specific rabbit polyclonal antibody that targets Recombining binding protein suppressor of hairless (RBP-J) and has been tested in ChIP-seq, Chromatin Immunoprecipitation (ChIP), and Western Blotting.
Chromatin Immunoprecipitation Analysis: A representative lot detected RBP-J in human T-cell acute lymphoblastic leukemia (T-ALL) cell line CUTLL1 (Wang, H., et. al. (2011). Proc Natl Acad Sci USA. 108(36):14908-13).
Western Blotting Analysis A 1:2,000 dilution from a representative lot detected RBP-J in GM12878 lymphoblasts (Courtesy of Dr Zhao Bo).
ChIP-seq Analysis: A representative lot detected RBP-J in ChIP-seq applications (Wang, H., et. al. (2011). Proc Natl Acad Sci USA. 108(36):14908-13).
Western Blotting Analysis: A representative lot detected RBPJ in T-cell acute lymphoblastic leukemia (T-ALL) cell lines of both human (KOPT-K1 , HPB-ALL, and CUTLL1) and murine (T6E and G4A2) origins) (Wang, H., et. al. (2011). Proc Natl Acad Sci USA. 108(36):14908-13).
Chip-seq Analysis: A representative lot detected RBPJ in GM12878 cells (Courtesy of Dr Zhao Bo).
Western Blotting Analysis A 1:2,000 dilution from a representative lot detected RBP-J in GM12878 lymphoblasts (Courtesy of Dr Zhao Bo).
ChIP-seq Analysis: A representative lot detected RBP-J in ChIP-seq applications (Wang, H., et. al. (2011). Proc Natl Acad Sci USA. 108(36):14908-13).
Western Blotting Analysis: A representative lot detected RBPJ in T-cell acute lymphoblastic leukemia (T-ALL) cell lines of both human (KOPT-K1 , HPB-ALL, and CUTLL1) and murine (T6E and G4A2) origins) (Wang, H., et. al. (2011). Proc Natl Acad Sci USA. 108(36):14908-13).
Chip-seq Analysis: A representative lot detected RBPJ in GM12878 cells (Courtesy of Dr Zhao Bo).
Research Category
Epigenetics & Nuclear Function
Epigenetics & Nuclear Function
Research Sub Category
Nuclear Receptors
Nuclear Receptors
품질
Evaluated by Western Blotting in HEK293 cell lysate.
Western Blotting Analysis: A 1:5,000 dilution of this antibody detected RBPJ in 10 µg of HEK293 cell lysate.
Western Blotting Analysis: A 1:5,000 dilution of this antibody detected RBPJ in 10 µg of HEK293 cell lysate.
표적 설명
~65 kDa observed; 55.64 kDa calculated. Uncharacterized bands may be observed in some lysate(s).
물리적 형태
Rabbit polyclonal in serum with 0.05% sodium azide.
Unpurified
저장 및 안정성
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
기타 정보
Concentration: Please refer to lot specific datasheet.
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
적합한 제품을 찾을 수 없으신가요?
당사의 제품 선택기 도구.을(를) 시도해 보세요.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Genome-wide analysis reveals conserved and divergent features of Notch1/RBPJ binding in human and murine T-lymphoblastic leukemia cells.
Proceedings of the National Academy of Sciences of the USA null
Communications biology, 3(1), 363-363 (2020-07-11)
Histone H3.3 mutations are a hallmark of pediatric gliomas, but their core oncogenic mechanisms are not well-defined. To identify major effectors, we used CRISPR-Cas9 to introduce H3.3K27M and G34R mutations into previously H3.3-wildtype brain cells, while in parallel reverting the
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.