LONP1 Antikörper

Produktnummer ABIN6569664

Produktdetails anti-LONP1 Antikörper

Target: LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LONP1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human LONP1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu LONP1

Target: LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

Andere Bezeichnung: LONP1 (LONP1 Produkte)

Synonyme: PRSS15 antikoerper, prss15 antikoerper, fc64d11 antikoerper, wu:fc64d11 antikoerper, LON antikoerper, LONP antikoerper, LonHS antikoerper, PIM1 antikoerper, hLON antikoerper, 1200017E13Rik antikoerper, Prss15 antikoerper, Lon antikoerper, lon peptidase 1, mitochondrial antikoerper, ATP-dependent Lon protease antikoerper, LONP1 antikoerper, lonp1 antikoerper, Lonp1 antikoerper, PIM1 antikoerper

Hintergrund:

Synonyms: hLON,hLON ATP dependent protease,LON,lon peptidase 1,mitochondrial,LON protease,Lon protease homolog,Lon protease like protein,Lon protease-like protein,LONHs,LONM,LONP,Lonp1,MGC1498,mitochondrial,Mitochondrial ATP dependent protease Lon,Mitochondrial ATP-dependent protease Lon,Mitochondrial lon peptidase 1,PIM1,Protease serine 15,PRSS15,Serine protease 15

Background: This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene.

Molekulargewicht:

Observed_MW: 105kDa

Calculated_MW: 85kDa/100kDa/106kDa

Gen-ID: 9361

UniProt: P36776