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Merck

P0497

Sigma-Aldrich

Anti-PMP70 antibody produced in rabbit

enhanced validation

affinity isolated antibody, buffered aqueous solution

Synonym(e):

Anti-70 kDa Peroxisomal membrane Protein, Anti-ABCD3, Anti-PXMP1

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About This Item

MDL-Nummer:
UNSPSC-Code:
12352203
NACRES:
NA.41

Biologische Quelle

rabbit

Qualitätsniveau

Konjugat

unconjugated

Antikörperform

affinity isolated antibody

Antikörper-Produkttyp

primary antibodies

Klon

polyclonal

Form

buffered aqueous solution

Mol-Gew.

antigen 70 kDa

Speziesreaktivität

human, mouse, rat

Erweiterte Validierung

independent
Learn more about Antibody Enhanced Validation

Methode(n)

immunoprecipitation (IP): 1-2 μg using RIPA extract (0.5 mg) from human HepG2 cells
indirect immunofluorescence: 4-8 μg/mL using mouse NIH3T3 cells
western blot (chemiluminescent): 0.5-1 μg/mL using whole extracts of rat PC12 cells or rat kidney extract or rat liver extract

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... ABCD3(5825)
mouse ... Abcd3(19299)
rat ... Abcd3(25270)

Allgemeine Beschreibung

The 70 kDa peroxisomal membrane protein (PMP70) is a major component of peroxisomal membranes. The peroxisome is a multifunctional single-membrane organelle associated with eukaryotic cells. PMP70 belongs to the ATP binding cassette (ABC) transporter superfamily.

Immunogen

synthetic peptide corresponding to amino acid residues 644-659 of rat PMP70 with N-terminal added cysteine, conjugated to KLH. The corresponding sequence is identical in mouse and differs by one amino acid in human.

Anwendung

Anti-PMP70 antibody produced in rabbit has been used in:
  • immunocytochemistry
  • immunostaining
  • immunofluorescence
  • western blotting
  • immunoprecipitation

Biochem./physiol. Wirkung

PMP70 participates in the metabolic transport of long and very long fatty acids into peroxisomes. PMP70 interacts and forms a stable complex with the adrenoleukodystrophy protein(ALDP), and also with several other peroxisomal proteins. ATP binding/hydrolysis by PMP70 and ALDL and their phosphorylation are involved in the regulation of fatty acid transport into peroxisomes. Mutations in the PMP70 (PXMP1) gene may cause a subset of Zellweger syndrome, an autosomal recessive disorder and is characterized by defects in import mechanism for peroxisomal matrix enzymes.

Physikalische Form

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

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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Lagerklassenschlüssel

10 - Combustible liquids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome
Gartner J, et al.
Nature Genetics, 1(1), 16-16 (1992)
Direct membrane association drives mitochondrial fission by the Parkinson disease-associated protein alpha-synuclein
Nakamura K, et al.
Test, 286(23), 20710-20726 (2011)
The impact of disparate isolation methods for extracellular vesicles on downstream RNA profiling
Van D, et al.
Journal of Extracellular Vesicles, 3(1), 24858-24858 (2014)
The 70-kDa peroxisomal membrane protein (PMP70) an ATP-binding cassette transporter
Imanaka T, et al.
Cell Biochemistry and Biophysics, 32(1-3), 131-138 (2000)
Jan Van Deun et al.
Journal of extracellular vesicles, 3 (2014-10-16)
Despite an enormous interest in the role of extracellular vesicles, including exosomes, in cancer and their use as biomarkers for diagnosis, prognosis, drug response and recurrence, there is no consensus on dependable isolation protocols. We provide a comparative evaluation of

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