LRIT3 Antikörper (AA 50-573)

Produktnummer ABIN7875413

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch LRIT3 in WB, ELISA und IF. Es zeigt Reaktivität gegenüber Proben von Human, Maus und Ratte.

Kurzübersicht für LRIT3 Antikörper (AA 50-573) (ABIN7875413)

Target: LRIT3 (Leucine-Rich Repeat, Immunoglobulin-Like and Transmembrane Domains 3 (LRIT3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LRIT3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Produktdetails anti-LRIT3 Antikörper

Bindungsspezifität: AA 50-573

Verwendungszweck: LRIT3 Antibody

Aufreinigung: Antigen affinity purified

Immunogen: An E.coli-derived human recombinant protein (amino acids E50-R573) was used as the immunogen for the LRIT3 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the LRIT3 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the LRIT3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu LRIT3

Target: LRIT3 (Leucine-Rich Repeat, Immunoglobulin-Like and Transmembrane Domains 3 (LRIT3))

Andere Bezeichnung: LRIT3

Hintergrund: Leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 is a protein that in humans is encoded by the LRIT3 gene. This gene encodes a protein that has a fibronectin type III domain and a C-terminal transmembrane domain, as well as a leucine-rich repeat domain and immunoglobulin-like domain near the N-terminus. The encoded protein may regulate fibroblast growth factor receptors and affect the modification of these receptors, which are glycosylated differently in the Golgi and endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night blindness, type 1F.

UniProt: Q3SXY7