LRPPRC anticorps (AA 1281-1394)

N° du produit ABIN7870417

Cet anticorps anti-LRPPRC Polyclonal Lapin (ABIN7870417) détecte spécifiquement LRPPRC dans WB, ELISA, IF, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris, Rat et Singe.

Aperçu rapide pour LRPPRC anticorps (AA 1281-1394) (ABIN7870417)

Antigène: LRPPRC (Leucine-Rich PPR-Motif Containing (LRPPRC))

Reactivité: Humain, Souris, Rat, Singe

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LRPPRC est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Détail du produit anti-LRPPRC anticorps

Épitope: AA 1281-1394

Fonction: LRPPRC Antibody / GP130

Purification: Affinity purified

Immunogène: Recombinant human protein (amino acids A1281-S1394) was used as the immunogen for the LRPPRC antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the LRPPRC antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the LRPPRC antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur LRPPRC

Antigène: LRPPRC (Leucine-Rich PPR-Motif Containing (LRPPRC))

Autre désignation: LRPPRC

Sujet: Leucine-rich PPR motif-containing protein, mitochondrial is a protein that in humans is encoded by the LRPPRC gene. It is mapped to 2p21. This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome.

UniProt: P42704