BBS2 Polyclonal Antibody | G-AB-11681

BBS2 Polyclonal Antibody | G-AB-11681 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Metabolism, Neuroscience

Synonyms: BBS2, BBS, RP74

Reactivity: Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 583

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human BBS2 (NP_114091.3) .

Clone #:

Conjugation: Unconjugated

Swissprot: Q9BXC9

Santa Cruz:

Calculated MW: 79 kDa

Observed MW: 100 kDa

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: WB

Dilution: WB 1:500-1:2000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

BBS2 Polyclonal Antibody DataSheet