Modification Site
None
C18orf56 Antibody, ALEXA FLUOR 594
Description:
Size: 100ul
Catalog no.: bs-9675R-A594
Price: 380 EUR
Product details
Crossreactivity
Human
Gene ID Number
494514
Target Antigen
C18orf56
Tested applications
IF(IHC-P)
French translation
anticorps
Clonality
Polyclonal
Modification
Unmodified
Concentration
1ug per 1ul
Excitation emission
590nm/617nm
Conjugated with
ALEXA FLUOR® 594
Conjugated
Alexa conjugate 1
Clone
Polyclonal antibody
Recommended dilutions
IF(IHC-P)(1:50-200)
Purification
Purified by Protein A.
Category
Conjugated Primary Antibodies
Conjugation
Alexa Fluor,ALEXA FLUOR® 594
Host Organism
Rabbit (Oryctolagus cuniculus)
Also known as
Anti-C18orf56 PAb ALEXA FLUOR 594
Specificity
This is a highly specific antibody against C18orf56.
Synonyms
Putative uncharacterized protein C18orf56; CR056_HUMAN.
Long name
C18orf56 Polyclonal Antibody, ALEXA FLUOR 594 Conjugated
Cross-reactive species details
Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
Source
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human C18orf56
Storage conditions
Store this antibody in aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Keep refrigerated at 2 to 8 degrees Celcius for up to one year.
Properties
For facs or microscopy Alexa 1 conjugate.If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies. ALEXA FLUOR they should be stored frozen at - 24°C for long term storage and for short term at + 5°C.
Background of the antigen
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.