Thermo Fisher 44-297G 抗体,Phospho-CREB (Ser129, Ser133) Polyclonal Antibody/Phospho-CREB(Ser129,Ser133)多克隆抗体

2024-10-23

Phospho-CREB (Ser129, Ser133) Polyclonal Antibody/Phospho-CREB(Ser129,Ser133)多克隆抗体

货号:44-297G

规格:100 µL

价格:4692

产品类型:抗体和染料

品牌:Thermo Fisher

抗原:Phosphopeptide containing amino acid sequence RRP[

物种:人/小鼠

宿主:兔

抗体亚型:IgG

荧光染料:其它

类型:多抗同型对照:
浓度: 用法:10 µL(ChIP);1:100-1:500(ICC);1:100-1:500(IF);1:1000(WB)
靶标信息CREB (Cyclic AMP response element binding protein) is a 43 kDa basic/leucine zipper transcription factor that binds the cyclic AMP response element (CRE) and activates transcription in response to a variety of extracellular signals including neurotransmitters, hormones, membrane depolarization, and growth and neurotrophic factors. Activation of CREB is dependent upon the phosphorylation of serine 133. Phosphorylation of CREB occurs via p44/42 MAP kinase and p90RSK, and via p38 MAP kinase and MSK1. Although CREB will bind DNA independent of its phosphorylation state, only the phosphorylated form is competent as a transcription factor. CREB binding protein (CBP), a transcriptional coactivator that directly interacts with CREB, binds to CREB in the region of serine 133. CREB is involved in different cellular processes including the synchronization of circadian rhythmicity, differentiation of adipose cells, and learning and memory. In humans, the gene is located on the q arm of chromosome 2. Diseases associated with CREB dysfunction include Alzheimer's Disease, histiocytoma and soft tissue melanoma.
数据:

Phospho-CREB (Ser129, Ser133) Antibody (44-297G) in IFImmunofluorescent analysis of CREB (pS129/pS133) was done on 70% confluent log phase HeLa cells. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.25% Triton™ X-100 for 10 minutes, and blocked with 5% BSA for 1 hour at room temperature. The cells were labeled with CREB (pS129/pS133) Rabbit polyclonal Antibody (Product # 44-297G) at 2 µg/mL in 1% BSA and incubated for 3 hours at room temperature and then labeled with Alexa Fluor 488 Goat Anti-Rabbit IgG Secondary Antibody (Product # A-11008) at a dilution of 1:400 for 30 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI (Product # S36938). F-actin (Panel c: red) was stained with Alexa Fluor 594 Phalloidin (Product # A12381). Panel d is a merged image showing nuclear localization. Panel e shows no primary antibody control. The images were captured at 20X magnification.

Phospho-CREB (Ser129, Ser133) Antibody (44-297G) in WBWhole cell extracts of human A549 cells (approximately 20,000 cells per lane) untreated (1), stimulated with EGF (2) or treated with pervanadate (3), were resolved by SDS-PAGE and transferred to PVDF. The membrane was blocked with a casein/Tween 20 buffer, then incubated with mouse anti-CREB/ATF1 (pS133) antibody (Product # 44-297G) at 0.5 µg/mL for 1 hour at room temperature. After washing, the membrane was incubated with an anti-mouse HRP-conjugated secondary antibody and signals were detected using an ECL detection method (exposure time: 30 seconds).
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