BBS2 rabbit pAb

BBS2 rabbit pAb

Item number: ES18093
Availability: In Stock
$148.00
$148.00
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Size: 50μL
Subtotal: $148.00
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BBS2 rabbit pAb

BBS2 rabbit pAb

$148.00

BBS2 rabbit pAb

$148.00
Size: 50μL
Product weight
0.005kg
Reactivity
Human; Mouse;Rat
Applications
WB
Source
Rabbit
Recommended dilutions
WB 1:500-2000
Immunogen
Synthesized peptide derived from human BBS2 AA range: 149-199
Isotype
IgG
Clonality
Polyclonal
Concentration
1 mg/ml
Geneid human
583
Human swiss prot no
Q9BXC9
Cellular localization
Cell projection, cilium membrane. Cytoplasm. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriolar satellite.
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.[provided by RefSeq, Oct 2014],

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