SIM1 Antikörper (N-Term)

Produktnummer ABIN2846084

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SIM1 in WB und IHC (p). Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für SIM1 Antikörper (N-Term) (ABIN2846084)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SIM1 Antikörper ist unkonjugiert

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

Klon: RB32160

Produktdetails anti-SIM1 Antikörper

Bindungsspezifität: AA 1-30, N-Term

Homologie: Zf, M, D

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

Immunogen: 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.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. WB: 1:2000. IHC-P-Leica: 1:250. IHC-P-Leica: 1:250

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 6 months

Details zu SIM1

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

Andere Bezeichnung: SIM1

Hintergrund: 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.

Gen-ID: 6492

NCBI Accession: NP_005059

UniProt: P81133