Modification Site
None
C1orf96 Antibody, ALEXA FLUOR 555
Description:
Size: 100ul
Catalog no.: bs-9796R-A555
Price: 380 EUR
Product details
Gene ID Number
126731
Target Antigen
C1orf96
Tested applications
IF(IHC-P)
French translation
anticorps
Clonality
Polyclonal
Modification
Unmodified
Concentration
1ug per 1ul
Excitation emission
553nm/568nm
Conjugated with
ALEXA FLUOR® 555
Crossreactivity
Human, Mouse, Rat
Clone
Polyclonal antibody
Recommended dilutions
IF(IHC-P)(1:50-200)
Purification
Purified by Protein A.
Conjugation
Alexa Fluor,ALEXA FLUOR 555
Category
Conjugated Primary Antibodies
Host Organism
Rabbit (Oryctolagus cuniculus)
Also known as
Anti-C1orf96 PAb ALEXA FLUOR 555
Specificity
This is a highly specific antibody against C1orf96.
Long name
C1orf96 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.
Source
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human C1orf96
Synonyms
C1orf96; FLJ37296; FLJ41471; Uncharacterized protein C1orf96; CCSAP_HUMAN; Centriole, cilia and spindle-associated protein; CCSAP; CSAP; RP4-803J11.3.
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
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf96 gene product has been provisionally designated C1orf96 pending further characterization.