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Merck
CN

SAB4200094

抗-PKM2 (亚型 M1) 兔抗

~1.5 mg/mL, affinity isolated antibody

别名:

抗-OIP3(OPA相互作用蛋白3), 抗-PK3, 抗-PKM, 抗-TCB, 抗-THBP1 (甲状腺激素结合蛋白,胞质), 抗-丙酮酸激酶,肌肉(亚型 M1)

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关于此项目

NACRES:
NA.44
UNSPSC Code:
12352203
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产品名称

抗-PKM2 (亚型 M1) 兔抗, ~1.5 mg/mL, affinity isolated antibody

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~60 kDa

species reactivity

human, rat, mouse

enhanced validation

recombinant expression
Learn more about Antibody Enhanced Validation

concentration

~1.5 mg/mL

technique(s)

immunocytochemistry: 5-10 μg/mL using HeLa cells
immunohistochemistry: 20-30 μg/mL using formalin-fixed paraffin embedded human colon
immunoprecipitation (IP): 2-4 μg using rat brain extract (S2 fraction)
western blot: 1-2 μg/mL using mouse brain extract (S2 fraction)

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... PKM2(5315)

Application

PKM2(同种型M1)抗体还可用于:
  • 免疫印迹
  • 免疫沉淀
  • 免疫组化
  • 免疫细胞化学

Biochem/physiol Actions

丙酮酸激酶(PK) 是糖酵解途径中的关键酶。研究证明,人类癌细胞系中M2 同种型的敲低及其被 M1 同种型替代会导致 Warburg 效应的逆转,并降低在小鼠异种移植物中形成肿瘤的能力。M2 同种型Tyr105 处 的磷酸化会抑制其活性,并且在人类癌症中很常见,这表明 Tyr105 是癌细胞中促进肿瘤发生的关键代谢开关(metabolic switch)。
抗 PKM2 (同种型M1) 抗体对人类、小鼠和大鼠 PKM2(同种型M1)/PKM1 有特异性。在免疫印迹中,PKM2(同种型M1)/PKM1条带的检测被免疫肽特异性抑制。

Disclaimer

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的人类或动物食用或应用。

General description

丙酮酸激酶(PK)是糖酵解的关键调节酶,具有四种同种型:L、R、M1和M2。同种型M2与癌转移有关。PK 同种型 M1 在胚胎发育过程中表达,是心脏、脑和骨骼肌组织中的主要同种型。

Physical form

0.01M磷酸盐缓冲盐水溶液,pH 7.4,含有15 mM叠氮化钠。

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存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mohammed Alquraishi et al.
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Human Molecular Genetics, 25(18), 4021-4040 (2016)
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The Journal of clinical investigation, 128(12), 5573-5586 (2018-10-05)
Notch signaling critically controls cell fate decisions in mammals, both during embryogenesis and in adults. In the skeleton, Notch suppresses osteoblast differentiation and sustains bone marrow mesenchymal progenitors during postnatal life. Stabilizing mutations of Notch2 cause Hajdu-Cheney syndrome, which is
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