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anti-Bardet-Biedl Syndrome 10 (BBS10) Antibodies

BBS10 is a member of the Bardet-Biedl syndrome (BBS) gene family. Additionally we are shipping BBS10 Proteins (3) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
BBS10 79738 Q8TAM1
BBS10 500832  
BBS10 71769 Q9DBI2
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Top anti-BBS10 Antibodies at

Showing 10 out of 49 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated FACS, WB Western blot analysis of BBS10 Antibody (C-term) (ABIN651074) in NCI-H460 cell line lysates (35 µg/lane). BBS10 (arrow) was detected using the purified polyclonal antibody. BBS10 Antibody (C-term) (ABIN651074) flow cytometric analysis of NCI-H460 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis. 400 μL Log in to see 10 to 11 Days
Human Rabbit Un-conjugated WB WB Suggested Anti-BBS10 Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:62500Positive Control: 293T cell lysate WB Suggested Anti-BBS10  Antibody Titration: 0.2-1 µg/mL ELISA Titer: 1:.2500  Positive Control:.93T cell lysate  BBS10 is supported by BioGPS gene expression data to be expressed in HEK293T 100 μL Log in to see 2 to 3 Days
Human Rabbit Un-conjugated IHC (p), WB IHC-P Image Immunohistochemical analysis of paraffin-embedded NCI-N87 xenograft, using BBS10, antibody at 1:500 dilution. WB Image Sample (30 ug of whole cell lysate) A: Hep G2 , 7.5% SDS PAGE antibody diluted at 1:1000 100 μL Log in to see 2 to 3 Days
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
Human Rabbit FITC FACS, ELISA, WB   200 μL Log in to see 8 to 10 Days
Human Rabbit Un-conjugated IHC (fp), WB 100 μL Log in to see 6 to 11 Days
Human Mouse Un-conjugated IF, WB Western Blot analysis of BBS10 expression in transfected 293T cell line by BBS10 MaxPab polyclonal antibody.Lane 1: FLJ23560 transfected lysate(16.61 KDa).Lane 2: Non-transfected lysate. Immunofluorescence of purified MaxPab antibody to BBS10 on HeLa cell. [antibody concentration 10 ug/ml] 50 μL Log in to see 9 Days
Human Rabbit Un-conjugated IHC, IHC (p) Immunohistochemistry: BBS10 Antibody [NBP2-32399] - Immunohistochemical staining of human bronchus shows strong positivity in ciliated cells of respiratory epithelia. Immunohistochemistry: BBS10 Antibody [NBP2-32399] - bronchus 0.1 mL Log in to see 8 to 11 Days
Human Rabbit Un-conjugated IHC (p), WB   100 μL Log in to see 8 to 10 Days
Human Rabbit Un-conjugated ELISA   200 μL Log in to see 8 to 10 Days

BBS10 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
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Rat (Rattus) ,

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Top referenced anti-BBS10 Antibodies

  1. Human Polyclonal BBS10 Primary Antibody for FACS, WB - ABIN651074 : Marion, Stoetzel, Schlicht, Messaddeq, Koch, Flori, Danse, Mandel, Dollfus: Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation. in Proceedings of the National Academy of Sciences of the United States of America 2009 (PubMed)

More Antibodies against BBS10 Interaction Partners

Human Bardet-Biedl Syndrome 10 (BBS10) interaction partners

  1. we report here, for the first time, in Indian population, a novel, different profile of mutations in BBS (show BBS2 Antibodies) genes (BBS3, BBS9 (show BBS9 Antibodies), BBS10 and BBS2 (show BBS2 Antibodies)) compared to worldwide (BBS1 (show BBS1 Antibodies) and 10) reports.

  2. novel BBS10 mutations in Bardet-Biedl syndrome patients in Spain

  3. Novel mutation (c.1181_1182insGCATTTATACC) in BBS10 (p.S396Lfs*6) found in Tunisian families with Bardet-Biedl syndrome.

  4. We report two affected brothers from a consanguineous Pakistani Punjabi family, both the brothers were homozygous for c.1958_1967del, which is a novel deletion in BBS10 that is likely to be causing the Bardet-Biedl syndrome in this family.

  5. Mutations identified in the present study extend the body of evidence implicating the genes ARL6 (show ARL4D Antibodies) and BBS10 in causing Bardet-Biedl syndrome.

  6. This study confirms the high frequency of BBS10 mutations, particularly of the p.Cys91LeufsX5 allele in Bardet-Biedl syndrome.

  7. Mutation in BBS10 modulates Bardet-Biedl syndrome in a sibling.

  8. Using sequence analysis, the role of BBS6 (show MKKS Antibodies), 10 and 12 was assessed in a Bardet-Biedl syndrome patient population comprising 93 cases from 74 families.

  9. the BBS10 and BBS12 (show BBS12 Antibodies) proteins are located within the basal body of this primary cilium and inhibition of their expression impairs ciliogenesis, activates the GSK3 (show GSK3b Antibodies) pathway, and induces PPAR (show PPARA Antibodies) nuclear accumulation, hence favoring adipogenesis

Mouse (Murine) Bardet-Biedl Syndrome 10 (BBS10) interaction partners

  1. report a major new BBS (show BBS2 Antibodies) locus, BBS10, that encodes a previously unknown, rapidly evolving vertebrate-specific chaperonin (show HSPD1 Antibodies)-like protein

  2. These findings confirm that FLJ23560 (BBS10) mutations are a significant cause of BBS (show BBS2 Antibodies).

BBS10 Antigen Profile

Protein Summary

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, 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 is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10.

Gene names and symbols associated with BBS10

  • Bardet-Biedl syndrome 10 (BBS10) antibody
  • Bardet-Biedl syndrome 10 (bbs10) antibody
  • Bardet-Biedl syndrome 10 (Bbs10) antibody
  • Bardet-Biedl syndrome 10 (human) (Bbs10) antibody
  • 1300007O09Rik antibody
  • AI452285 antibody
  • C12orf58 antibody
  • MGC84945 antibody
  • RGD1560748 antibody
  • si:dkey-30c15.16 antibody

Protein level used designations for BBS10

Bardet-Biedl syndrome 10 , Chaperonin Containing TCP-1 family member (cct-1)-like , Bardet-Biedl syndrome 10 protein , Bardet-Biedl syndrome 10 protein homolog

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734282 Xenopus laevis
100034535 Danio rerio
100145168 Xenopus (Silurana) tropicalis
79738 Homo sapiens
500832 Rattus norvegicus
100173034 Pongo abelii
71769 Mus musculus
Selected quality suppliers for anti-BBS10 (BBS10) Antibodies
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