GLTPD2 Antikörper (Alexa Fluor 594)

Produktnummer ABIN2813797

Produktdetails anti-GLTPD2 Antikörper

Target: GLTPD2 (Glycolipid Transfer Protein Domain Containing 2 (GLTPD2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GLTPD2 Antikörper ist konjugiert mit Alexa Fluor 594

Applikation: Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLTPD2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu GLTPD2

Target: GLTPD2 (Glycolipid Transfer Protein Domain Containing 2 (GLTPD2))

Andere Bezeichnung: GLTPD2 (GLTPD2 Produkte)

Synonyme: C730027E14Rik antikoerper, RP23-122P1.9 antikoerper, RGD1560459 antikoerper, glycolipid transfer protein domain containing 2 antikoerper, GLTPD2 antikoerper, Gltpd2 antikoerper

Hintergrund:

The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5 % of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Synonyms: glycolipid transfer protein domain-containing protein 2, Glycolipid transfer protein domain containing 2, GLTD2_HUMAN.