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Merck
CN

04-953

抗磷酸化-Smad2(Ser465/467)抗体,克隆A5S,兔单克隆

culture supernatant, clone A5S, Upstate®

别名:

Anti-Anti-CHTD8, Anti-Anti-JV18, Anti-Anti-JV18-1, Anti-Anti-LDS6, Anti-Anti-MADH2, Anti-Anti-MADR2, Anti-Anti-hMAD-2, Anti-Anti-hSMAD2

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
A5S, monoclonal
Species reactivity:
human, zebrafish, mouse, canine
Application:
western blot
Technique(s):
western blot: suitable
Citations:
30
Uniprot accession no.:
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产品名称

抗磷酸化-Smad2(Ser465/467)抗体,克隆A5S,兔单克隆, culture supernatant, clone A5S, Upstate®

biological source

rabbit

antibody form

culture supernatant

antibody product type

primary antibodies

clone

A5S, monoclonal

species reactivity

human, zebrafish, mouse, canine

manufacturer/tradename

Upstate®

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

phosphorylation (pSer465/pSer467)

Quality Level

Gene Information

human ... SMAD2(4087)

Analysis Note

对照
HL60细胞裂解液,经TGFa处理的HepG2细胞或经TGF处理的HepG2细胞β
已通过免疫印迹分析进行常规评估。

Application

使用抗磷酸化Smad2(Ser465/467)抗体,克隆A5S(兔单克隆抗体)检测磷酸化Smad2(Ser465/467),该抗体已证明可在WB中发挥作用。

Biochem/physiol Actions

根据序列同源性预测与非洲爪蟾发生交叉反应。
识别磷酸化Smad2。与Smad3没有交叉反应。

General description

55-60 kDa
SMAD2或MAD-mothers against decapentaplegic-homolog是一种多肽,顾名思义,是果蝇基因:“Mothers against decepentaplegic”的同系物它属于SMAD蛋白家族,该家族又属于TGFb调节子超家族。像其他许多TGFb家族成员一样,SMAD2液参与细胞信号转导的调节。SMAD2可调节激活素和TGFb′s的信号。它可与SMAD锚相互作用激活受体(SARA)。配体的结合会引起SMAD2蛋白的磷酸化,从而与SARA的解离并与SMAD4缔合。随后,它被转移至细胞核,与其他蛋白质形成复合物并充当转录因子。SMAD2是受受体调节的SMAD(R-SMAD),并由骨形态发生蛋白1型受体激酶激活。

Immunogen

对应于人Smad2 Ser465/467位点周围氨基酸[pS]M[pS]的KLH偶联合成肽

Other Notes

替代:05-953
浓度:请参考批次特异性浓缩物的分析证书。

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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存储类别

10 - Combustible liquids

wgk

WGK 2


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Oddrun Elise Olsen et al.
PloS one, 12(11), e0187349-e0187349 (2017-11-22)
Purified recombinant proteins for use in biomedical research are invaluable to investigate protein function. However, purity varies in protein batches made in mammalian expression systems, such as CHO-cells or HEK293-cells. This study points to caution while investigating effects of proteins
Linjia Jiang et al.
The Journal of experimental medicine, 215(5), 1337-1347 (2018-04-20)
Cell cycle quiescence is critical for hematopoietic stem cell (HSC) maintenance. TGF-β signaling in bone marrow niche has been identified in regulating HSC quiescence; however, the intrinsic regulatory mechanisms remain unclear. This study reports that Shp-1 knockout HSCs have attenuated
Cathepsin K expression and activity in canine osteosarcoma.
J M Schmit,H C Pondenis,A M Barger,L B Borst,L D Garrett,J M Wypij,Z L Neumann,T M Fan
Journal of Veterinary Internal Medicine null
Amrita Chatterjee et al.
Cancer letters, 360(2), 134-140 (2015-02-11)
The mammalian target of rapamycin complex 1 (mTORC1) is a critical regulator of G1 cell cycle progression. Two key substrates of mTORC1 are ribosomal subunit S6 kinase (S6K) and eukaryotic initiation factor 4E (eIF4E) binding protein-1 (4E-BP1). We reported previously
Elena Sierra-Filardi et al.
Blood, 117(19), 5092-5101 (2011-03-11)
M-CSF favors the generation of folate receptor β-positive (FRβ⁺), IL-10-producing, immunosuppressive, M2-polarized macrophages [M2 (M-CSF)], whereas GM-CSF promotes a proinflammatory, M1-polarized phenotype [M1 (GM-CSF)]. In the present study, we found that activin A was preferentially released by M1 (GM-CSF) macrophages

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