SIM1 anticorps (N-Term)

N° du produit ABIN656884

Cet anticorps Lapin Polyclonal détecte spécifiquement SIM1 dans WB et IHC (p). Il présente une réactivité envers Humain.

Aperçu rapide pour SIM1 anticorps (N-Term) (ABIN656884)

Antigène: SIM1 (Single-Minded Homolog 1 (SIM1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SIM1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB32160

Détail du produit anti-SIM1 anticorps

Épitope: AA 1-30, N-Term

Homologie: Zf, M, D

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

Immunogène: This SIM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human SIM1.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:2000. IHC-P-Leica: 1:250. IHC-P-Leica: 1:250

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: SIM1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur SIM1

Antigène: SIM1 (Single-Minded Homolog 1 (SIM1))

Autre désignation: SIM1

Sujet: SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.

ID gène: 6492

NCBI Accession: NP_005059

UniProt: P81133