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# AF3184, RRID:AB_2834616.
展开/折叠
Anemia, X-linked, without thrombocytopenia, included; ERYF 1; Eryf1; Erythroid transcription factor; Erythrold transcription factor 1; GATA 1; GATA binding factor 1; GATA binding protein 1 (globin transcription factor 1); GATA binding protein 1; GATA-1; GATA-binding factor 1; GATA1; GATA1_HUMAN; GF 1; GF-1; GF1; Globin transcription factor 1; NF E1; NF E1 DNA binding protein; NF-E1 DNA-binding protein; NFE 1; NFE1; Nuclear factor erythroid 1; Transcription factor GATA1; XLANP; XLTDA; XLTT;
抗原和靶标
- P15976 GATA1_HUMAN:
- Protein BLAST With
- NCBI/
- ExPASy/
- Uniprot
MEFPGLGSLGTSEPLPQFVDPALVSSTPESGVFFPSGPEGLDAAASSTAPSTATAAAAALAYYRDAEAYRHSPVFQVYPLLNCMEGIPGGSPYAGWAYGKTGLYPASTVCPTREDSPPQAVEDLDGKGSTSFLETLKTERLSPDLLTLGPALPSSLPVPNSAYGGPDFSSTFFSPTGSPLNSAAYSSPKLRGTLPLPPCEARECVNCGATATPLWRRDRTGHYLCNACGLYHKMNGQNRPLIRPKKRLIVSKRAGTQCTNCQTTTTTLWRRNASGDPVCNACGLYYKLHQVNRPLTMRKDGIQTRNRKASGKGKKKRGSSLGGTGAAEGPAGGFMVVAGGSGSGNCGEVASGLTLGPPGTAHLYQGLGPVVLSGPVSHLMPFPGPLLGSPTGSFPTGPMPPTTSTTVVAPLSS
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 - P15976 作为底物
Site | PTM Type | Enzyme | Source |
---|---|---|---|
S26 | Phosphorylation | P27361 (MAPK3) | Uniprot |
S72 | Phosphorylation | Uniprot | |
Y78 | Phosphorylation | Uniprot | |
S91 | Phosphorylation | Uniprot | |
S116 | Phosphorylation | Uniprot | |
S131 | Phosphorylation | Uniprot | |
K137 | Sumoylation | Uniprot | |
S142 | Phosphorylation | Uniprot | |
S161 | Phosphorylation | Q9P286 (PAK5) | Uniprot |
S178 | Phosphorylation | Uniprot | |
S187 | Phosphorylation | Q9P286 (PAK5) | Uniprot |
Y223 | Phosphorylation | Uniprot | |
Y231 | Phosphorylation | Uniprot | |
K233 | Acetylation | Uniprot | |
K245 | Acetylation | Uniprot | |
K246 | Acetylation | Uniprot | |
Y285 | Phosphorylation | Uniprot | |
Y286 | Phosphorylation | Uniprot | |
T304 | Phosphorylation | Uniprot | |
S310 | Phosphorylation | P31749 (AKT1) | Uniprot |
K312 | Acetylation | Uniprot | |
K314 | Acetylation | Uniprot | |
K315 | Acetylation | Uniprot | |
K316 | Acetylation | Uniprot | |
S319 | Phosphorylation | Uniprot | |
S320 | Phosphorylation | Uniprot | |
T324 | Phosphorylation | Uniprot |
研究背景
Transcriptional activator or repressor which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence 5'-[AT]GATA[AG]-3' within regulatory regions of globin genes and of other genes expressed in erythroid cells. Activates the transcription of genes involved in erythroid differentiation of K562 erythroleukemia cells, including HBB, HBG1/2, ALAS2 and HMBS.
Highly phosphorylated on serine residues. Phosphorylation on Ser-310 is enhanced on erythroid differentiation. Phosphorylation on Ser-142 promotes sumoylation on Lys-137 (By similarity).
Sumoylation on Lys-137 is enhanced by phosphorylation on Ser-142 and by interaction with PIAS4. Sumoylation with SUMO1 has no effect on transcriptional activity (By similarity).
Acetylated at 2 conserved lysine-rich motifs by CREBBP in vitro. Acetylation does not affect DNA-binding in vitro but is essential to induce erythroid differentiation and for binding chromatin in vivo (By similarity). Acetylated on Lys-233, Lys-245 Lys-246 by EP300.
Nucleus.
Erythrocytes.
May form homodimers or heterodimers with other isoforms. Interacts (via the N-terminal zinc finger) with ZFPM1. Interacts with GFI1B. Interacts with PIAS4; the interaction enhances sumoylation and represses the transactivational activity in a sumoylation-independent manner. Interacts with LMCD1. Interacts with BRD3 (By similarity). Interacts with CREBBP; the interaction stimulates acetylation and transcriptional activity in vivo (By similarity). Interacts with EP300. Interacts with MED1, CCAR1 and CALCOCO1. Interacts with CEBPE.
The two fingers are functionally distinct and cooperate to achieve specific, stable DNA binding. The first finger is necessary only for full specificity and stability of binding, whereas the second one is required for binding (By similarity).
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