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Product Name
MKS1 antibody
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Description
MKS1 Rabbit Polyclonal antibody. Positive IF detected in hTERT-RPE1 cells and Mouse embryonic fibroblasts. Positive IHC detected in human liver cancer tissue, human ovary tissue. Positive WB detected in mouse brain tissue, HEK-293 cells, HeLa cells, mouse uterus tissue, SH-SY5Y cells. Positive IP detected in HEK-293 cells. Observed molecular weight by Western-blot: 65-70 kDa
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Tested applications
ELISA, WB, IHC, IF, IP
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Species reactivity
Human,Mouse,Rat; other species not tested.
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Alternative names
BBS13 antibody; FLJ20345 antibody; Meckel syndrome type 1 protein antibody; Meckel syndrome antibody; type 1 antibody; MES antibody; MKS antibody; MKS1 antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of MKS1 recombinant protein (Accession Number: BC010061). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IP: 1:500-1:5000
IHC: 1:20-1:200
IF: 1:20-1:200
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Validations
mouse brain tissue were subjected to SDS PAGE followed by western blot with Catalog No:112670(BBS13 antibody) at dilution of 1:1000
IP Result of anti-BBS13 (IP:Catalog No:112670, 3ug; Detection:Catalog No:112670 1:1000) with HEK-293 cells lysate 4500ug.
Immunohistochemical of paraffin-embedded human liver cancer using Catalog No:112670(BBS13 antibody) at dilution of 1:50 (under 10x lens)
Immunohistochemical of paraffin-embedded human liver cancer using Catalog No:112670(BBS13 antibody) at dilution of 1:50 (under 40x lens)
IF result from Dr. Corbit, Kevin. anti-MKS1(Catalog No:112670) marks the transition zone of Human hTERT-RPE1 cells and Mouse embryonic fibroblasts.
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Background
MKS1 (Meckel syndrome type 1 protein) is a 559-amino acid protein that contains a conserved B9 domain. It is a component of a large protein complex which localizes to the ciliary transition zone and regulates mammalian ciliogenesis and ciliary membrane composition (PMID: 21725307). MKS1 is required for ciliary structure and function, and is involved in centrosome migration to the apical cell surface during early ciliogenesis (PMID: 17185389; 19515853). Broad tissue expression of the MKS1 gene has been reported (PMID: 16415886). Defects in MKS1 are the cause of Meckel syndrome type 1 (MKS1), an autosomal recessive lethal malformation syndrome characterized by renal cystic dysplasia, central nervous system malformations, and hepatic developmental defects (PMID: 16415886). In addition, defects in MKS1 are also the cause of Bardet-Biedl syndrome type 13 (BBS13) (PMID: 18327255).
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References
- Garcia-Gonzalo FR, Corbit KC, Sirerol-Piquer MS. A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition. Nature genetics. 43(8):776-84. 2011.
- Goetz SC, Liem KF, Anderson KV. The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis. Cell. 151(4):847-58. 2012.
- Nozawa YI, Yao E, Lin C. Fused (Stk36) is a ciliary protein required for central pair assembly and motile cilia orientation in the mammalian oviduct. Developmental dynamics : an official publication of the American Association of Anatomists. 242(11):1307-19. 2013.
- Hall EA, Keighren M, Ford MJ. Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes. PLoS genetics. 9(12):e1003928. 2013.
- Yang Y, Ran J, Liu M. CYLD mediates ciliogenesis in multiple organs by deubiquitinating Cep70 and inactivating HDAC6. Cell research. 24(11):1342-53. 2014.
- Bangs FK, Schrode N, Hadjantonakis AK, Anderson KV. Lineage specificity of primary cilia in the mouse embryo. Nature cell biology. 17(2):113-22. 2015.
- Roberson EC, Dowdle WE, Ozanturk A. TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone. The Journal of cell biology. 209(1):129-42. 2015.
- Ran J, Yang Y, Li D, Liu M, Zhou J. Deacetylation of α-tubulin and cortactin is required for HDAC6 to trigger ciliary disassembly. Scientific reports. 5:12917. 2015.
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