Name: Goat Anti Human EMAP-II polyclonal, antigen affinity
SKU: RKAP038
Availability: InStock


accession	Q12904

Applications	ELISA:This antibody can be used at 2 μg/mL jointly with biotinylated Human EMAP-II antibody to detect Human EMAP-II. The detection limit for recombinant Human EMAP-II is approximately 0.2 ng/well. Western Blot:This antibody can be used at 0.2 μg/mL with the appropriate secondary reagents to detect Human EMAP-II. The detection limit for recombinant Human EMAP-II is approximately 0.2 ng/lane.
Source	This antibody was produced in rabbits immunized with recombinant Human EMAP-II.
Species reactivity	Human
Purification	The specific antibody was purified from Goat sera by using immobilized recombinant Human EMAP-II affinity chromatography.
Presentation	Lyophilized from PBS, pH 7.2.
Storage	The lyophilized antibody is stable for at least 1 year from date of receipt at -20° C. Upon reconstitution, this antibody can be stored in working aliquots at 2° - 8° C for one month, or at -20° C for 12 months without detectable loss of activity. Avoid repeated freeze/thaw cycles.
Usage	This antibody product is for research purposes only.It may not be used for therapeutics or diagnostic purposes.

Biological Process	Angiogenesis
Biological Process	Carbohydrate-metabolism
Biological Process	Cell-adhesion
Molecular function	Cytokine
Molecular function	RNA-binding


Sandwich ELISA 96-well maxisorp plates were coated with the capture antibody overnight, then blocked with 5% FCS in PBS for 1 hour, then washed. Then, the protein standard was added, and plates were incubated for 2 hrs at 37°C. Plates were washed and incubated with a biotinylated detection antibody for 1 hour at 37°C. After washing, plates were incubated with HRP-conjugated streptavidin for 30 min at room temperature and washed again. Plates were developed using the tetramethylbenzidine peroxidase substrate system and absorbance was measured at 450-615 nm using an automated plate reader.
Western Blot The Recombinant immunogen was migrated by 12% SDS-PAGE and transferred to a 0.2 um PVDF membrane. After blocking the membrane in blocking buffer (5% milk powder in 20 mM Tris-HCl pH 7.5, 500 mM NaCl, 0.1% (v/v) Tween 20 , the membrane was incubated with primary antibody ( at 4°C overnight. Peroxidase-linked secondary anti-rabbit were used to detect the bound primary antibodies. Enhanced chemiluminescence (ECL) reagents were used to visualize

Goat Anti Human EMAP-II polyclonal, antigen affinity

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