Product Name: AITRL Antibody
Species Reactivity: Human
Tested Applications: ELISA, WB
Applications: ELISA:Indirect:To detect hAITRL by indirect ELISA (using 100 μL/well antibody solution) a concentration of 0.5 – 2.0 μg/mL of this antibody is required. This antigen affinity purified antibody, in conjunction with compatible secondary reagents, allows the detection of at least 0.2 – 0.4 ng/well of recombinant hAITRLSandwichTo detect hAITRL by sandwich ELISA (using 100 μL/well antibody solution) a concentration of 0.5 – 2.0 μg/mL of this antibody is required. This antigen affinity purified antibody, in conjunction with our biotinylated Anti-Human AITRL as a detection antibody, allows the detection of at least 0.2 – 0.4 ng/well of recombinant hAITRL. Western Blot:To detect hAITRL by Western Blot analysis this antibody can be used at a concentration of 0.1 – 0.2 μg/mL. Used in conjunction with compatible secondary reagents the detection limit for recombinant hAITRL is 1.5 – 3.0 ng/lane, under either reducing or non-reducing conditions.
User Note: Centrifuge vial prior to opening.
Predicted Molecular Weight:
Immunogen: Produced from sera of rabbits pre-immunized with highly pure (>98%) recombinant hAITRL. Human AITRL specific antibody was purified by affinity chromatography employing immobilized hAITRL matrix.
Host Species: Rabbit
Purification:
Physical State: Lyophilized
CAS NO.: 1820565-69-2
Product: PIM-447 (dihydrochloride)
Buffer:
Concentration:
Storage Conditions: AITRL antibody is stable for at least 2 years from date of receipt at -20˚C. The reconstituted antibody is stable for at least two weeks at 2-8˚C. Frozen aliquots are stable for at least 6 months when stored at -20˚C. Avoid repeated freeze-thaw cycles.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: TL6, AITRL, GITRL, hGITRL, TL6, UNQ149/PRO175, Tumor necrosis factor ligand superfamily member 18, Activation-inducible TNF-related ligand
Accession NO.: Q9UNG2
Protein Ino: 325511353
Official Symbol: TNFSF18
Geneid: 8995
Background:
PubMed ID:http://aac.asm.org/content/52/7/2581.abstract
