MKS1 Polyclonal Antibody (E-AB-19009)

For research use only.
Verified Samples |
Verified Samples in WB: Mouse liver, Jurkat Verified Samples in IHC: Human brain |
Dilution | WB 1:500-1:2000, IHC 1:30-1:150 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC |
Clonality | Polyclonal |
Immunogen | Fusion protein of human MKS1 |
Abbre | MKS1 |
Synonyms | B8d3, BBS13, Dysencephalia splanchnocystica, FABB proteome like protein, FLJ20345, Gruber syndrome, Meckel gruber syndrome, Meckel gruber syndrome type 1, Meckel syndrome, Meckel syndrome type 1, Meckel syndrome type 1 protein, Meckel syndrome type 1 protein homolog |
Swissprot | |
Calculated MW | 65 kDa |
Observed MW |
Refer to figures
The actual band is not consistent with the expectation.
Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane. |
Cellular Localization | Cytoplasm>cytoskeleton>cilium basal body. Cytoplasm>cytoskeleton>microtubule organizing center>centrosome. Localizes at the transition zone, a region between the basal body and the ciliary axoneme. |
Concentration | 0.9 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Antigen affinity purification |
Research Areas | Tags, Cell Markers |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | 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. |
Other Clones
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Unconjugated
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