BBS2 293T Cell Transient Overexpression Lysate(Denatured)
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More Files
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SDS-PAGE Gel
BBS2 transfected lysate.
Western Blot
Lane 1: BBS2 transfected lysate ( 79.9 KDa)
Lane 2: Non-transfected lysate.
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Specification
Transfected Cell Line
293T
Plasmid
pCMV-BBS2 full-length
Host
Human
Theoretical MW (kDa)
79.9
Interspecies Antigen Sequence
Mouse (90); Rat (90)
Quality Control Testing
Transient overexpression cell lysate was tested with Anti-BBS2 antibody (H00000583-B01) by Western Blots.
SDS-PAGE Gel
BBS2 transfected lysate.
Western Blot
Lane 1: BBS2 transfected lysate ( 79.9 KDa)
Lane 2: Non-transfected lysate.Storage Buffer
1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot
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Gene Info — BBS2
Entrez GeneID
583GeneBank Accession#
BC014140.2Protein Accession#
AAH14140.1Gene Name
BBS2
Gene Alias
BBS, MGC20703
Gene Description
Bardet-Biedl syndrome 2
Gene Ontology
HyperlinkGene Summary
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 six other BBS proteins
Other Designations
Bardet-Biedl syndrome 2 protein
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Interactome
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Disease
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