产品: | DDX5 抗体 |
货号: | DF7539 |
描述: | Rabbit polyclonal antibody to DDX5 |
应用: | WB IHC |
反应: | Human, Mouse, Rat |
预测: | Pig, Bovine, Horse, Sheep, Dog |
分子量: | 69 kDa; 69kD(Calculated). |
蛋白号: | P17844 |
RRID: | AB_2841038 |
产品描述
*The optimal dilutions should be determined by the end user.
*Tips:
WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.
引用格式: Affinity Biosciences Cat# DF7539, RRID:AB_2841038.
展开/折叠
ATP dependent RNA helicase DDX5; DDX 5; Ddx5; DDX5_HUMAN; DEAD (Asp Glu Ala Asp) box helicase 5; DEAD (Asp Glu Ala Asp) box polypeptide 5; DEAD box 5; DEAD box protein 5; DEAD/H (Asp Glu Ala Asp/His) box polypeptide 5 (RNA helicase, 68kD); G17P1; HELR; HLR1; HUMP68; P68; p68 RNA helicase; Probable ATP dependent RNA helicase DDX5; Probable ATP-dependent RNA helicase DDX5; RNA helicase p68;
抗原和靶标
- P17844 DDX5_HUMAN:
- Protein BLAST With
- NCBI/
- ExPASy/
- Uniprot
MSGYSSDRDRGRDRGFGAPRFGGSRAGPLSGKKFGNPGEKLVKKKWNLDELPKFEKNFYQEHPDLARRTAQEVETYRRSKEITVRGHNCPKPVLNFYEANFPANVMDVIARQNFTEPTAIQAQGWPVALSGLDMVGVAQTGSGKTLSYLLPAIVHINHQPFLERGDGPICLVLAPTRELAQQVQQVAAEYCRACRLKSTCIYGGAPKGPQIRDLERGVEICIATPGRLIDFLECGKTNLRRTTYLVLDEADRMLDMGFEPQIRKIVDQIRPDRQTLMWSATWPKEVRQLAEDFLKDYIHINIGALELSANHNILQIVDVCHDVEKDEKLIRLMEEIMSEKENKTIVFVETKRRCDELTRKMRRDGWPAMGIHGDKSQQERDWVLNEFKHGKAPILIATDVASRGLDVEDVKFVINYDYPNSSEDYIHRIGRTARSTKTGTAYTFFTPNNIKQVSDLISVLREANQAINPKLLQLVEDRGSGRSRGRGGMKDDRRDRYSAGKRGGFNTFRDRENYDRGYSSLLKRDFGAKTQNGVYSAANYTNGSFGSNFVSAGIQTSFRTGNPTGTYQNGYDSTQQYGSNVPNMHNGMNQQAYAYPATAAAPMIGYPMPTGYSQ
种属预测
score>80的预测可信度较高,可尝试用于WB检测。*预测模型主要基于免疫原序列比对,结果仅作参考,不作为质保凭据。
High(score>80) Medium(80>score>50) Low(score<50) No confidence
翻译修饰 - P17844 作为底物
Site | PTM Type | Enzyme | Source |
---|---|---|---|
S2 | Phosphorylation | Uniprot | |
S5 | Phosphorylation | Uniprot | |
S6 | Phosphorylation | Uniprot | |
R10 | Methylation | Uniprot | |
R12 | Methylation | Uniprot | |
R14 | Methylation | Uniprot | |
R20 | Methylation | Uniprot | |
S24 | Phosphorylation | Uniprot | |
R25 | Methylation | Uniprot | |
S30 | Phosphorylation | Uniprot | |
K32 | Acetylation | Uniprot | |
K32 | Ubiquitination | Uniprot | |
K33 | Acetylation | Uniprot | |
K33 | Ubiquitination | Uniprot | |
K40 | Acetylation | Uniprot | |
K40 | Ubiquitination | Uniprot | |
K43 | Acetylation | Uniprot | |
K44 | Acetylation | Uniprot | |
K45 | Acetylation | Uniprot | |
K45 | Sumoylation | Uniprot | |
K45 | Ubiquitination | Uniprot | |
K53 | Acetylation | Uniprot | |
K53 | Sumoylation | Uniprot | |
K53 | Ubiquitination | Uniprot | |
K56 | Acetylation | Uniprot | |
K56 | Methylation | Uniprot | |
K56 | Sumoylation | Uniprot | |
K56 | Ubiquitination | Uniprot | |
Y59 | Phosphorylation | Uniprot | |
S79 | Phosphorylation | Uniprot | |
K80 | Acetylation | Uniprot | |
K80 | Ubiquitination | Uniprot | |
T83 | Phosphorylation | Uniprot | |
K91 | Ubiquitination | Uniprot | |
Y97 | Phosphorylation | Uniprot | |
K144 | Ubiquitination | Uniprot | |
K197 | Methylation | Uniprot | |
K197 | Ubiquitination | Uniprot | |
S198 | Phosphorylation | P49137 (MAPKAPK2) | Uniprot |
T199 | Phosphorylation | Uniprot | |
C200 | S-Nitrosylation | Uniprot | |
Y202 | Phosphorylation | Uniprot | |
K207 | Sumoylation | Uniprot | |
K207 | Ubiquitination | Uniprot | |
T224 | Phosphorylation | Uniprot | |
C234 | S-Nitrosylation | Uniprot | |
K236 | Acetylation | Uniprot | |
K236 | Ubiquitination | Uniprot | |
T243 | Phosphorylation | Uniprot | |
Y244 | Phosphorylation | Uniprot | |
R263 | Methylation | Uniprot | |
K264 | Acetylation | Uniprot | |
K264 | Ubiquitination | Uniprot | |
R273 | Methylation | Uniprot | |
S279 | Phosphorylation | Uniprot | |
K284 | Ubiquitination | Uniprot | |
Y297 | Phosphorylation | Uniprot | |
K328 | Ubiquitination | Uniprot | |
S338 | Phosphorylation | Uniprot | |
K340 | Acetylation | Uniprot | |
K340 | Methylation | Uniprot | |
K340 | Ubiquitination | Uniprot | |
K343 | Ubiquitination | Uniprot | |
T344 | Phosphorylation | Uniprot | |
K351 | Acetylation | Uniprot | |
K351 | Ubiquitination | Uniprot | |
K375 | Ubiquitination | Uniprot | |
K388 | Acetylation | Uniprot | |
K388 | Ubiquitination | Uniprot | |
K391 | Sumoylation | Uniprot | |
K391 | Ubiquitination | Uniprot | |
S402 | Phosphorylation | Uniprot | |
R403 | Methylation | Uniprot | |
K411 | Sumoylation | Uniprot | |
K411 | Ubiquitination | Uniprot | |
Y416 | Phosphorylation | Uniprot | |
S421 | Phosphorylation | Uniprot | |
Y425 | Phosphorylation | Uniprot | |
K437 | Sumoylation | Uniprot | |
K437 | Ubiquitination | Uniprot | |
T438 | Phosphorylation | Uniprot | |
T440 | Phosphorylation | Uniprot | |
Y442 | Phosphorylation | Uniprot | |
T446 | Phosphorylation | Q16539 (MAPK14) | Uniprot |
K451 | Ubiquitination | Uniprot | |
S454 | Phosphorylation | Uniprot | |
S458 | Phosphorylation | Uniprot | |
K470 | Acetylation | Uniprot | |
K470 | Sumoylation | Uniprot | |
K470 | Ubiquitination | Uniprot | |
R478 | Methylation | Uniprot | |
S480 | Phosphorylation | Uniprot | |
R484 | Methylation | Uniprot | |
R486 | Methylation | Uniprot | |
K490 | Methylation | Uniprot | |
S498 | Phosphorylation | Uniprot | |
K501 | Acetylation | Uniprot | |
R502 | Methylation | Uniprot | |
T507 | Phosphorylation | Uniprot | |
R509 | Methylation | Uniprot | |
Y514 | Phosphorylation | Uniprot | |
R516 | Methylation | Uniprot | |
Y518 | Phosphorylation | Uniprot | |
S519 | Phosphorylation | Uniprot | |
S520 | Phosphorylation | Uniprot | |
K523 | Sumoylation | Uniprot | |
K523 | Ubiquitination | Uniprot | |
Y535 | Phosphorylation | Uniprot | |
S557 | Phosphorylation | Uniprot | |
T564 | Phosphorylation | Q16539 (MAPK14) | Uniprot |
Y593 | Phosphorylation | P00519 (ABL1) | Uniprot |
Y595 | Phosphorylation | Uniprot |
研究背景
Involved in the alternative regulation of pre-mRNA splicing; its RNA helicase activity is necessary for increasing tau exon 10 inclusion and occurs in a RBM4-dependent manner. Binds to the tau pre-mRNA in the stem-loop region downstream of exon 10. The rate of ATP hydrolysis is highly stimulated by single-stranded RNA. Involved in transcriptional regulation; the function is independent of the RNA helicase activity. Transcriptional coactivator for androgen receptor AR but probably not ESR1. Synergizes with DDX17 and SRA1 RNA to activate MYOD1 transcriptional activity and involved in skeletal muscle differentiation. Transcriptional coactivator for p53/TP53 and involved in p53/TP53 transcriptional response to DNA damage and p53/TP53-dependent apoptosis. Transcriptional coactivator for RUNX2 and involved in regulation of osteoblast differentiation. Acts as transcriptional repressor in a promoter-specific manner; the function probably involves association with histone deacetylases, such as HDAC1. As component of a large PER complex is involved in the inhibition of 3' transcriptional termination of circadian target genes such as PER1 and NR1D1 and the control of the circadian rhythms.
Arg-502 is dimethylated, probably to asymmetric dimethylarginine.
Sumoylated; sumoylation, promoted by PIAS1, promotes interaction with HDAC1 and transcriptional repression activity. Sumoylation also significantly increases stability, and reduces polyubiquitination.
Polyubiquitinated, leading to proteasomal degradation.
Nucleus>Nucleolus.
Identified in the spliceosome C complex. Interacts with RBM4; the interaction occurs in an RNA-independent manner. Interacts with AGO1 and AGO2. Interacts with ESR1, AR, EP300, CREBBP, POLR2A, TP53, RUNX2 and HDAC1. Self-associates. Interacts with DDX17. Interacts with BRDT. The large PER complex involved in the repression of transcriptional termination is composed of at least PER2, CDK9, DDX5, DHX9, NCBP1 and POLR2A (active). Interacts with DHX36; this interaction occurs in a RNA-dependent manner. Interacts with NUPR1 (By similarity). Interacts with ERCC6.
Belongs to the DEAD box helicase family. DDX5/DBP2 subfamily.
研究领域
· Genetic Information Processing > Transcription > Spliceosome.
· Human Diseases > Cancers: Overview > Transcriptional misregulation in cancer.
· Human Diseases > Cancers: Overview > Proteoglycans in cancer.
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