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BBS2 Rabbit Polyclonal Antibody

CAT: 0965-JOT-AP06280-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0965-JOT-AP06280-01Size:20 µL
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Background
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy| obesity| polydactyly| renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies| ciliary axonemes| and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.
CAS Number
9007-83-4
Synonyms
BBS2
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Synthesized peptide derived from human BBS2
Clonality
Polyclonal
Applications
WB
Stability
-20°C for 1 year
Concentration
1 mg/ml
Molecular Weight
79310
Antibody Type
Primary antibody
Isotype
IgG