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Invitrogen™ CC2D2A Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5100428
Description
Antibody detects endogenous levels of total CC2D2A.
This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants.
Specifications
CC2D2A | |
Polyclonal | |
Unconjugated | |
CC2D2A | |
5730509K17Rik; b2b1035Clo; CC2D2A; coiled-coil and C2 domain containing 2A; coiled-coil and C2 domain-containing protein 2A; JBTS9; KIAA1345; MKS6 | |
Rabbit | |
Affinity chromatography | |
RUO | |
231214, 57545 | |
-20°C | |
Liquid |
Western Blot | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q8CFW7, Q9P2K1 | |
CC2D2A | |
A synthesized peptide derived from human CC2D2A(Accession Q9P2K1), corresponding to amino acid residues V997-I1047. | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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