SCFD2 Antikörper (AA 20-585)

Produktnummer ABIN7871879

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch SCFD2 in WB, ELISA, FACS und IF. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für SCFD2 Antikörper (AA 20-585) (ABIN7871879)

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SCFD2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)

Produktdetails anti-SCFD2 Antikörper

Bindungsspezifität: AA 20-585

Verwendungszweck: SCFD2 Antibody / Sec1 family domain-containing protein 2

Aufreinigung: Antigen affinity purified

Immunogen: E. coli-derived recombinant human protein (amino acids K20-H585) was used as the immunogen for the SCFD2 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the SCFD2 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 SCFD2 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 SCFD2

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Andere Bezeichnung: SCFD2

Hintergrund: SCFD2 (sec1 family domain containing 2), also known as STXBP1L1 (syntaxinbinding protein 1-like 1), is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntingtoni 1/2s disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease

UniProt: Q8WU76