LONP1 anticorps (AA 120-400)

N° du produit ABIN1680707

Détail du produit anti-LONP1 anticorps

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

Épitope: AA 120-400

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LONP1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)

Séquence: VFPHLPLIAI TRNPVFPRFI KIIEVKNKKL VELLRRKVRL AQPYVGVFLK RDDSNESDVV ESLDEIYHTG TFAQIHEMQD LGDKLRMIVM GHRRVHISRQ LEVEPEEPEA ENKHKPRRKS KRGKKEAEDE LSARHPAELA MEPTPELPAE VLMVEVENVV HEDFQVTEEV KALTAEIVKT IRDIIALNPL YRESVLQMMQ AGQRVVDNPI YLSDMGAALT GAESHELQDV LEETNIPKRL YKALSLLKKE FELSKLQQRL GREVEEKIKQ THRKYLLQEQ L

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 120-400 of human LONP1 (NP_004784.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200,IP,1:50 - 1:200

Restrictions: For Research Use only

Stockage

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur LONP1

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

Autre désignation: LONP1 (LONP1 Produits)

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

Sujet: 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.,LONP1,CODASS,LON,LONP,LonHS,PIM1,PRSS15,hLON,Epigenetics & Nuclear Signaling,Cancer,Endocrine & Metabolism,Mitochondrial metabolism,Nucleotide metabolism,LONP1

Poids moléculaire: 85 kDa/100 kDa/106 kDa

ID gène: 9361

UniProt: P36776