1ug per 1ul
ALEXA FLUOR® 647
Human, Mouse, Rat
Purified by Protein A.
Alexa Fluor,ALEXA FLUOR 647
Conjugated Primary Antibodies
Rabbit (Oryctolagus cuniculus)
Anti-CCDC25 PAb ALEXA FLUOR 647
This is a highly specific antibody against CCDC25.
CCDC25 Polyclonal Antibody, ALEXA FLUOR 647 Conjugated
Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
CCD25_HUMAN; CCDC25; coiled-coil domain containing 25; CCDC25 coiled coil domain containing 25.
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human CCDC25
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.
For facs or microscopy Alexa 1 conjugate.Alexa Fluor 633 is a practical alternative to APC as well as Cy5. Bioss Primary Conjugated Antibodies. ALEXA FLUOR made this Alexa Fluor 633 conjugate that can be used in multi-color flow cytometry with instruments equipped with a second red laser or red diode. It is detected in the FL4 detector of the core's upgraded 2-laser FACScans. Like other Alexa Fluor dyes, the Anti-CCDC25 exhibits uncommon photo stability, making it an ideal choice for fluorescent microscopy.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.
CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.