Modification Site
None
C2orf27 Antibody, ALEXA FLUOR 555
Description:
Size: 100ul
Catalog no.: bs-15148R-A555
Price: 380 EUR
Product details
Crossreactivity
Human
Target Antigen
C2orf27
French translation
anticorps
Tested applications
IF(IHC-P)
Modification
Unmodified
Clonality
Polyclonal
Excitation emission
553nm/568nm
Concentration
1ug per 1ul
Gene ID Number
29798 and 408029
Conjugated with
ALEXA FLUOR® 555
Recommended dilutions
IF(IHC-P)(1:50-200)
Clone
Polyclonal antibody
Purification
Purified by Protein A.
Conjugation
Alexa Fluor,ALEXA FLUOR 555
Category
Conjugated Primary Antibodies
Host Organism
Rabbit (Oryctolagus cuniculus)
Also known as
Anti-C2orf27 PAb ALEXA FLUOR 555
Specificity
This is a highly specific antibody against C2orf27.
Long name
C2orf27 Polyclonal Antibody, ALEXA FLUOR 555 Conjugated
Cross-reactive species details
Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
Synonyms
C2orf27A; Chromosome 2 open reading frame 27A; MGC50273; OTTHUMP00000162444; Uncharacterized protein C2orf27.
Source
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human C2orf27
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.Very high photo stable ALEXA 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
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf27 gene product has been provisionally designated C2orf27 pending further characterization.