MKS1 产品
(Meckel Syndrome, Type 1 (MKS1))
Categories
The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009].
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Featured MKS1 Categories
Recommended MKS1 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IF, FACS
Validations
- (3)
Cat. No.
ABIN6244194
Quantity
200 μL
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC, IP
Validations
- (2)
Cat. No.
ABIN7159091
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, ELISA, IHC
Validations
- (2)
Cat. No.
ABIN7247090
Quantity
200 μL
Datasheet
Datasheet
Recommended MKS1 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3083864
Quantity
1 mg
Datasheet
Datasheet
Reactivity
Mouse
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3135236
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our MKS1 Products
: "Dishevelled stabilization by the ciliopathy protein Rpgrip1l is essential for planar cell polarity." in: The Journal of cell biology, Vol. 198, Issue 5, pp. 927-40, (2012) (PubMed).Synonyms and alternative names related to MKS1
Meckel syndrome, type 1 (MKS1), Meckel syndrome, type 1 (Mks1), AK190930, B8d3, BBS13, MES, MKS, POC12Protein level used designations for MKS1
- FABB proteome-like protein
- Meckel syndrome type 1 protein
- POC12 centriolar protein homolog
- Meckel syndrome type 1 protein homolog
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