HSPA5 Antibody, Unconjugated, Rabbit, Polyclonal

Artikelnummer: PRS-57-011
Artikelname: HSPA5 Antibody, Unconjugated, Rabbit, Polyclonal
Artikelnummer: PRS-57-011
Hersteller Artikelnummer: 57-011
Alternativnummer: PRS-57-011-200
Hersteller: ProSci
Wirt: Rabbit
Kategorie: Antikörper
Applikation: FC, IF, IHC-P, WB
Spezies Reaktivität: Human, Mouse
Immunogen: This HSPA5 antibody is generated from rabbits immunized with a recombinant protein encoding full length human HSPA5.
Konjugation: Unconjugated
Alternative Synonym: 78 kDa glucose-regulated protein, GRP-78, Endoplasmic reticulum lumenal Ca(2+)-binding protein grp78, Heat shock 70 kDa protein 5, Immunoglobulin heavy chain-binding protein, BiP, HSPA5, GRP78
Klonalität: Polyclonal
Konzentration: batch dependent
Molekulargewicht: 72 kDa
NCBI: 3309
UniProt: P11021
Puffer: Supplied in PBS with 0.09% (W/V) sodium azide.
Formulierung: Liquid
Application Verdünnung: Optimal dilutions for each application to be determined by the researcher.
Anwendungsbeschreibung: For WB starting dilution is: 1:1000For IHC-P starting dilution is: 1:50~100For IF starting dilution is: 1:10~50For FACS starting dilution is: 1:10~50
Antibody is used in Western blot to detect HSPA5 in mouse liver tissue lysate. HSPA5 (arrow) was detected using the purified Pab.
Western blot analysis of anti-HSPA5 Pab in HL60 cell line lysates (35ug/lane).
Formalin-fixed and paraffin-embedded human prostata carcinoma tissue reacted with HSPA5 antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining.
Formalin-fixed and paraffin-embedded human Testis tissue reacted with HSPA5 antibody , which was peroxidase-conjugated to the secondary antibody, followed by AEC staining.
Confocal immunofluorescent analysis of HSPA5 Antibody with NCI-H460 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
Flow cytometric analysis of Hela cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.