INCENP Rabbit Polyclonal Antibody

CAT#: TA890129

Rabbit Polyclonal anti-INCENP Antibody

Size: 30 ul 100 ul


 

USD 407.00

In Stock*

Size
    • 100 ul

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Frequently bought together (2)
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Specifications

Product Data
Applications WB
Recommended Dilution WB: 1:500~2000
Reactivities Human, Rat, Mouse
Host Rabbit
Isotype IgG
Clonality Polyclonal
Immunogen Recombinant protein of human INCENP
Formulation PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration 3.23 mg/ml
Purification Purified from the immunized serum by affinity chromatography (Protein A/G)
Conjugation Unconjugated
Storage Store at -20°C as received.
Stability Stable for 12 months from date of receipt.
Predicted Protein Size 105.2 kDa
Gene Name inner centromere protein
Background In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger,' or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (centromere protein A; MIM 117139), CENPB (MIM 117140), CENPC1 (MIM 117141), and CENPD (MIM 117142). The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle (Earnshaw and Mackay, 1994 [PubMed 8088460]). These include CENPE (MIM 117143); MCAK (MIM 604538); KID (MIM 603213); cytoplasmic dynein (e.g., MIM 600112); CliPs (e.g., MIM 179838); and CENPF/mitosin (MIM 600236). The inner centromere proteins (INCENPs) (Earnshaw and Cooke, 1991 [PubMed 1860899]), the initial members of the passenger protein group, display a broad localization along chromosomes in the early stages of mitosis but gradually become concentrated at centromeres as the cell cycle progresses into mid-metaphase. During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis (Cutts et al., 1999 [PubMed 10369859]). [supplied by OMIM, Mar 2008]
Synonyms FLJ31633; MGC111393
Reference Data
Protein Families Druggable Genome

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