Pet1 Recombinant Rabbit Monoclonal Antibody [PSH07-77] - BSA and Azide free
Catalog# HA751189
Pet1 Recombinant Rabbit Monoclonal Antibody [PSH07-77] - BSA and Azide free
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WB
-
IF-Cell
-
IHC-P
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Human
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HA722893
含抗保成分
-
unconjugated
概述
产品名称
Pet1 Recombinant Rabbit Monoclonal Antibody [PSH07-77] - BSA and Azide free
抗体类型
Recombinant Rabbit monoclonal Antibody
免疫原
Recombinant protein within human Pet1 aa 137-238.
种属反应性
Human
验证应用
WB, IF-Cell, IHC-P
分子量
Predicted band size:
偶联
unconjugated
克隆号
PSH07-77
产品特性
形态
Liquid
浓度
存放说明
Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
存储缓冲液
1*PBS (pH7.4).
亚型
IgG
纯化方式
Protein A affinity purified.
应用稀释度
-
WB
-
1:2,000
-
IF-Cell
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1:50,000
-
IHC-P
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1:10,000
靶点
功能
Functions as a transcriptional regulator. According to 1, it functions as a transcriptional repressor. Functions in the differentiation and the maintenance of the central serotonergic neurons. May play a role in cell growth. This gene belongs to the ETS transcription factor family. ETS family members have a highly conserved 85-amino acid ETS domain that binds purine-rich DNA sequences. The alanine-rich C-terminus of this gene indicates that it may act as a transcription repressor. This gene is exclusively expressed in neurons of the central serotonin (5-HT) system, a system implicated in the pathogeny of such psychiatric diseases as depression, anxiety, and eating disorders. In some types of Ewing tumors, this gene is fused to the Ewing sarcoma (EWS) gene following chromosome translocations.
背景文献
1. Aydin B et al. Foxa2 and Pet1 Direct and Indirect Synergy Drive Serotonergic Neuronal Differentiation. Front Neurosci. 2022 Jun
2. Barettino C et al. Developmental Disruption of Erbb4 in Pet1+ Neurons Impairs Serotonergic Sub-System Connectivity and Memory Formation. Front Cell Dev Biol. 2021 Dec
亚细胞定位
Nucleus.
UNIPROT
别名
ETS-domain transcription factor antibody
FEV (ETS oncogene family) antibody
FEV antibody
FEV ETS transcription factor antibody
FEV_HUMAN antibody
Fifth Ewing sarcoma variant antibody
Fifth Ewing variant protein antibody
HSRNAFEV antibody
mPet1 antibody
PC12 ETS domain-containing transcription factor 1 antibody
展开图片
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☑ Cell treatment (CT)
Western blot analysis of Pet1 on different lysates with Rabbit anti-Pet1 antibody (HA751189) at 1/2,000 dilution.
Lane 1: 293T transfected with empty control cell lysate
Lane 2: 293T transfected with Pet1 cell lysate
Lysates/proteins at 15 µg/Lane.
Predicted band size: 25 kDa
Observed band size: 30 kDa
Exposure time: 20 seconds; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA751189) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. -
☑ Cell treatment (CT)
Immunocytochemistry analysis of HeLa transfected with Pet1 cells labeling Pet1 with Rabbit anti-Pet1 antibody (HA751189) at 1/50,000 dilution.
Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Pet1 antibody (HA751189) at 1/50,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. -
☑ Cell treatment (CT)
Immunohistochemical analysis of paraffin-embedded HeLa transfected with Pet1 cells with Rabbit anti-Pet1 antibody (HA751189) at 1/10,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA751189) at 1/10,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
请注意: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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