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Merck
CN

P0084

Sigma-Aldrich

Monoclonal Anti-Pinin antibody produced in mouse

~1.5 mg/mL, clone 5F1, purified immunoglobulin, buffered aqueous solution

别名:

Anti-DRS, Anti-PNN, Anti-SDK3, Anti-memA

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UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

mouse

偶联物

unconjugated

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

5F1, monoclonal

表单

buffered aqueous solution

分子量

antigen ~140 kDa

种属反应性

monkey, bovine, human, canine

包装

antibody small pack of 25 μL

浓度

~1.5 mg/mL

技术

immunocytochemistry: suitable
indirect ELISA: suitable
western blot: 1-2 μg/mL using HeLa nuclear cell extract

同位素/亚型

IgG1

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... PNN(5411)

一般描述

Monoclonal Anti-Pinin (mouse IgG1 isotype) is derived from the hybridoma 5F1 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice. Pinin (PNN) is a serine/arginine-rich (SR)-related protein, that is found to localize to the cytoplasmic face of the desmosomal plaque in the convergence of intermediate filaments and to pin them to the desmosome. It consists of an Arg-Ser (RS) domain in its carboxyl terminus. This gene is mapped to human chromosome 14q.

免疫原

synthetic peptide corresponding to amino acids 547-737 of human pinin, conjugated to KLH.

应用

Monoclonal Anti-Pinin antibody produced in mouse may be used in:
  • enzyme-linked immunosorbent assay (ELISA)
  • immunoblotting
  • immunocytochemistry

生化/生理作用

Monoclonal Anti-Pinin recognizes human pinin. It crossreacts with monkey, bovine, and dog pinin.
Pinin (PNN) is mainly linked with the mature desmosomes of the epithelia. It plays a role in inducing junction formation and enhance cell aggregation. PNN transcription and protein levels were found to be reduced in renal and transitional cell carcinomas, suggesting its role as a tumor suppressor. PNN protein reduction by RNAi or knockdown resulted in loss of cell-cell adhesion as well as aberrant mouse development. It plays a key role in mRNA export, cell−cell adhesion, alternative splicing and cell migration. PNN also controls gene transcription.

外形

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

制备说明

For extended storage, freeze at -20 °C in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if notused within 12 hours.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Change in gene expression subsequent to induction of Pnn/DRS/memA: increase in p21 cip1/waf1
Shi Y, et al.
Oncogene, 20(30), 4007-4018 (2001)
Loss of Pnn expression results in mouse early embryonic lethality and cellular apoptosis through SRSF1-mediated alternative expression of Bcl-xS and ICAD
Leu S, et al.
Journal of Cell Science, 125(13), 3164-3172 (2012)
Alvin Wong et al.
Plastic and reconstructive surgery, 130(5), 1012-1021 (2012-10-26)
Infantile hemangiomas can cause significant morbidity during proliferation, yet there is no U.S. Food and Drug Administration-approved treatment. They are believed to form from hemangioma stem cells, which differentiate toward a hemangioma endothelial cell phenotype. Recently, propranolol has demonstrated effectiveness
Zhi Yu et al.
World journal of gastroenterology, 22(5), 1834-1843 (2016-02-09)
To investigate whether electroacupuncture (EA) at ST25 affects jejunal motility in vivo and if so, whether a sympathetic pathway is involved. Jejunal motility was assessed using a manometric balloon placed in the jejunum approximately about 3-5 cm away from the
Xuanming Hu et al.
BMC complementary and alternative medicine, 17(1), 329-329 (2017-06-24)
Gastrointestinal motility disorder has been demonstrated to be regulated by acupuncture treatment. The mechanisms underlying the effects of acupuncture stimulation of abdominal and lower limb acupoints on gastrointestinal motility have been thoroughly studied; however, the physiology underlying the effects of

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