Anti-BBS2 (N-terminal) polyclonal antibody

Rabbit Anti-Human BBS2 (N-terminal) polyclonal antibody for WB, IHC-P, IHC-Fr. 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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SPECIFICATIONS

Catalog Number

CABT-BL4211

Hosts

Rabbit

Reactivities

Hum, Mouse, Rat

Conjugates

Unconj

Target

BBS2

Gene Id

583

Isotype

IgG

Clonality

Polyclonal

Storage Temp

Store at 4В°C short term (1-2 weeks). Aliquot and store at -20В°C (add glycerol to a final volume of 40% for extra stability). Avoid repeated freeze/thaw cycles.