Kinetochore Scaffold 1 Peptide 1


Catalog Number:


Target Antigen:

Kinetochore Scaffold 1 Peptide 1




Rabbit Recombinant Cloned Antibody

Last Updated:


Antigen Recognition(s):

Peptide, Phosphorylation

Characterization Data [Compare Characterization Data]
Download This PDF contains the evaluation results provided by the Human Protein Atlas ( (288.5 KB)

CPTC-KNL1-1 Evaluation by the Human Protein Atlas

Result: Negative

This PDF contains the evaluation results provided by the Human Protein Atlas (

  IHC Tissue

CTPC-KNL1-1 IHC Tissue

Result: Negative

This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.


NCI Identification Number:


Antigen Name:

Kinetochore Scaffold 1 Peptide 1

CPTC Name:

CPTC-KNL1 Peptide 1


Kinetochore Scaffold 1; Cancer/Testis Antigen 29; Cancer Susceptibility Candidate Gene 5 Protein; ALL1-Fused Gene From Chromosome 15q14 Protein; Protein Phosphatase 1, Regulatory Subunit 55; Microcephaly, Primary Autosomal Recessive 4; Blinkin, Bub-Linking Kinetochore Protein; Cancer Susceptibility Candidate 5; Kinetochore-Null Protein 1; CASC5; CT29; Kinetochore Null 1 Homolog (C. Elegans); Bub-Linking Kinetochore Protein; Kinetochore Null 1 Homolog; Protein D40/AF15q14; Protein CASC5; KIAA1570; PPP1R55; HSpc105; AF15q14; Blinkin; HKNL-1; MCPH4; Spc7; D40


The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. KNL1 (Kinetochore Scaffold 1) is a Protein Coding gene. Diseases associated with KNL1 include Microcephaly 4, Primary, Autosomal Recessive and Primary Microcephaly. Among its related pathways are Signaling by Rho GTPases and Mitotic Metaphase and Anaphase.Performs two crucial functions during mitosis: it is essential for spindle-assembly checkpoint signaling and for correct chromosome alignment. Required for attachment of the kinetochores to the spindle microtubules. Directly links BUB1 and BUB1B to kinetochores. Part of the MIS12 complex, which may be fundamental for kinetochore formation and proper chromosome segregation during mitosis. Acts in coordination with CENPK to recruit the NDC80 complex to the outer kinetochore.

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DNA Source:



Synthetic Peptide

Vector Name:


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Expressed Sequence:


Native Sequence:

Calculated Isoelectric Point:

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Last Updated:



Characterization Data


No SOPs available.

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