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Merck

P0084

Sigma-Aldrich

Monoclonal Anti-Pinin antibody produced in mouse

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

Synonym(e):

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

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About This Item

UNSPSC-Code:
12352203
NACRES:
NA.41

Biologische Quelle

mouse

Konjugat

unconjugated

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

5F1, monoclonal

Form

buffered aqueous solution

Mol-Gew.

antigen ~140 kDa

Speziesreaktivität

monkey, bovine, human, canine

Verpackung

antibody small pack of 25 μL

Konzentration

~1.5 mg/mL

Methode(n)

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

Isotyp

IgG1

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... PNN(5411)

Allgemeine Beschreibung

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.

Spezifität

Monoclonal Anti-Pinin recognizes human pinin. It crossreacts with monkey, bovine, and dog pinin.

Immunogen

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

Anwendung

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

Biochem./physiol. Wirkung

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.

Physikalische Form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Lagerung und Haltbarkeit

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.

Haftungsausschluss

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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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
Mengqian Yuan et al.
Evidence-based complementary and alternative medicine : eCAM, 2016, 3840230-3840230 (2016-11-08)
Background. The roles of the sympathetic and parasympathetic systems in mediating the effect of electroacupuncture (EA) at ST37 on jejunal motility have yet to be demonstrated. Aim. We used rats and mice to investigate the effect and mechanism of action
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
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

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