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BBS5 Polyclonal antibody
BBS5 Polyclonal Antibody for IHC, IP, WB,ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse, rat
Applications
WB, IP, IHC, IF,ELISA
Conjugate
Unconjugated
Cat no : 14569-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | mouse retina tissue, mouse testis tissue, human testis tissue, rat testis tissue, mouse eye tissue |
Positive IP detected in | mouse testis tissue |
Positive IHC detected in | human testis tissue, mouse kidney tissue, human stomach tissue, human kidney tissue, mouse testis tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
Application | Dilution |
---|---|
Western Blot (WB) | WB : 1:500-1:1000 |
Immunoprecipitation (IP) | IP : 0.5-4.0 ug for IP and 1:500-1:1000 for WB |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
Sample-dependent, check data in validation data gallery |
Published Applications
KD/KO | See 2 publications below |
WB | See 10 publications below |
IHC | See 1 publications below |
IF | See 17 publications below |
Product Information
14569-1-AP targets BBS5 in WB, IP, IHC, IF,ELISA applications and shows reactivity with human, mouse, rat samples.
Tested Reactivity | human, mouse, rat |
Cited Reactivity | human, mouse, rat |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | BBS5 fusion protein Ag6153 |
Full Name | Bardet-Biedl syndrome 5 |
Calculated molecular weight | 39 kDa |
Observed molecular weight | 39 kDa |
GenBank accession number | BC044593 |
Gene symbol | BBS5 |
Gene ID (NCBI) | 129880 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
Background Information
BBS5 encodes a protein that has been directly linked to Bardet-Biedl syndrome. Bardet-Biedl syndrome (BBS) is an autosomal recessive condition characterised by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, hypogonadism, and renal dysfunction. Other associated clinical findings in BBS patients include diabetes, hypertension and congenital heart defects. BBS expression varies both within and between families and diagnosis is often difficult. Experimentation in non-human eukaryotes suggests that BBS5 is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized.
Protocols
Product Specific Protocols | |
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WB protocol for BBS5 antibody 14569-1-AP | Download protocol |
IHC protocol for BBS5 antibody 14569-1-AP | Download protocol |
IP protocol for BBS5 antibody 14569-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
Publications
Species | Application | Title |
---|---|---|
PLoS Biol Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.
| ||
Invest Ophthalmol Vis Sci Essential Role of the Chaperonin CCT in Rod Outer Segment Biogenesis. | ||
J Biol Chem DAZ interacting protein 1 (Dzip1) phosphorylation by Polo-like kinase 1 (Plk1) regulates the centriolar satellites localization of the BBSome during the cell cycle. |