MPV17 anticorps (C-Term)

N° du produit ABIN5517191

Cet anticorps anti-MPV17 Polyclonal Lapin (ABIN5517191) détecte spécifiquement MPV17 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour MPV17 anticorps (C-Term) (ABIN5517191)

Antigène: MPV17 (MpV17 Mitochondrial Inner Membrane Protein (MPV17))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MPV17 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-MPV17 anticorps

Épitope: C-Term

Fonction: MPV17 Antibody - C-terminal region

Séquence: LDQGGFAPCF LGCFLPLVGA LNGLSAQDNW AKLQRDYPDA LITNYYLWPA

Attributs du produit: This is a rabbit polyclonal antibody against MPV17. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C-terminal region of Human MPV17

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP73712-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur MPV17

Antigène: MPV17 (MpV17 Mitochondrial Inner Membrane Protein (MPV17))

Autre désignation: MPV17

Sujet:

Background Information: This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS).

Alternative Symbols: SYM1, CMT2EE, MTDPS6

Poids moléculaire: 19kDa

ID gène: 4358

NCBI Accession: XP_005264383

UniProt: P39210

Pathways: Sensory Perception of Sound