SVOPL anticorps (AA 241-269)

N° du produit ABIN1538165

L’anticorps anti-SVOPL Polyclonal Lapin est utilisé pour la détection de SVOPL dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour SVOPL anticorps (AA 241-269) (ABIN1538165)

Antigène: SVOPL (SVOP-Like (SVOPL))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SVOPL est non-conjugé

Application: Western Blotting (WB)

Clone: RB35924

Détail du produit anti-SVOPL anticorps

Épitope: AA 241-269

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SVOPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 241-269 amino acids from the Central region of human SVOPL.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: SVOPL Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur SVOPL

Antigène: SVOPL (SVOP-Like (SVOPL))

Autre désignation: SVOPL

Sujet: SVOPL (putative transporter SVOPL), also known as SV2-related protein-like, is a 492 amino acid multi-pass membrane protein belonging to the major facilitator superfamily. SVOPL is a paralog to synaptic vesicle protein (SVOP) that exists as two alternatively spliced isoforms. The gene encoding SVOPL maps to human chromosome 7q34. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up approximately 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Deletions of portions of the q arm of chromosome 7 are linked to myeloid disorders, including acute myelogenous leukemia and myelodysplasia.

Poids moléculaire: 53991

ID gène: 136306

NCBI Accession: NP_001132928, NP_777619

UniProt: Q8N434