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BBS2 Antibody

CAT: 0223-22-928Size: 100 µLDry Ice: NoHazardous: No
CAT#:0223-22-928Size:100 µL
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PRICE
AVAILABILITY: InStock
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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.
NCBI Gene ID
583
Swiss Prot
Q9BXC9
Host
Rabbit
Reactivity
Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-96 of human BBS2 (NP_114091.3) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Cell Cycle, Neuroscience
Purification
Affinity purification
Positive Control
Mouse testis
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 100kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
BBS2
Positive Control 2
Mouse liver
Positive Control 3
Mouse kidney
Positive Control 4
Rat liver
Positive Control 5
Rat brain
Positive Control 6
Rat lung
NCBI Official Name
Bardet-Biedl syndrome 2
NCBI Organism
Homo sapiens
Other Product Names
BBS, RP74, Bardet-Biedl syndrome 2 protein
Tested Applications
WB
Physical Properties
Liquid

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