Claudin 16 Antikörper (AA 50-150)

Produktnummer ABIN6138679

Produktdetails anti-Claudin 16 Antikörper

Target: Claudin 16 (CLDN16)

Bindungsspezifität: AA 50-150

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Claudin 16 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: HLSGARAGVC PCCHPDGLLA TMRDLLQYIA CFFAFFSAGF LIVATWTDCW MVNADDSLEV STKCRGLWWE CVTNAFDGIR TCDEYDSILA EHPLKLVVTR A

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 50-150 of human CLDN16 (NP_006571.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu Claudin 16

Target: Claudin 16 (CLDN16)

Andere Bezeichnung: CLDN16 (CLDN16 Produkte)

Synonyme: CLDN16 antikoerper, HOMG3 antikoerper, PCLN1 antikoerper, claudin-16 antikoerper, Pcln1 antikoerper, claudin 16 antikoerper, CLDN16 antikoerper, Cldn16 antikoerper

Hintergrund: Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is found primarily in the kidneys, specifically in the thick ascending limb of Henle, where it acts as either an intercellular pore or ion concentration sensor to regulate the paracellular resorption of magnesium ions. Defects in this gene are a cause of primary hypomagnesemia, which is characterized by massive renal magnesium wasting with hypomagnesemia and hypercalciuria, resulting in nephrocalcinosis and renal failure. This gene and the CLDN1 gene are clustered on chromosome 3q28.,CLDN16,HOMG3,PCLN1,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Tight Junctions,Cytoskeleton,CLDN16

Molekulargewicht: 33 kDa

Gen-ID: 10686

UniProt: Q9Y5I7

Pathways: Hepatitis C