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SAB4200128

Sigma-Aldrich

Anti-DYX1C1 (N-terminal) antibody produced in rabbit

enhanced validation

~1.5 mg/mL, affinity isolated antibody

Synonym(s):

Anti-DYX1, Anti-DYXC1, Anti-Dyslexia susceptibility 1 candidate 1, Anti-EKN1, Anti-RD

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~48 kDa

species reactivity

human

enhanced validation

recombinant expression
Learn more about Antibody Enhanced Validation

concentration

~1.5 mg/mL

technique(s)

western blot: 1-2 μg/mL using lysates of HEK-293T cells overexpressing human DYX1C1

shipped in

dry ice

Storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... DYX1C1(161582)

General description

Anti-DYX1C1 (N-terminal) is produced in rabbit using as the immunogen a synthetic peptide corresponding to a sequence at the N-terminal of human DYX1C1, conjugated to KLH. DYX1C1 is expressed in brain and the protein resides in the nucleus.
DYX1C1/dynein axonemal assembly factor 4 (DNAAF4) gene with 10 exons, extending over a length of ~78 kb on genomic DNA, is mapped to human chromosome 15q21.3. DYX1C1 contains a nuclear tetratricopeptide repeat domain.

Application

Anti-DYX1C1 (N-terminal) antibody produced in rabbit has been used in immunoblotting.
Anti-DYX1C1 (N-terminal) antibody produced in rabbit has been used in immunofluorescence studies.

Biochem/physiol Actions

DYX1C1 has been recently implicated as a cancer biomarker in colorectal cancer.
DYX1C1/dynein axonemal assembly factor 4 (DNAAF4) plays a vital role in neuronal migration and regulation of estrogen receptor signaling. Mutation in the gene increases the risk of susceptibility to developmental dyslexia (DD). Variations in the gene is also associated with the deficits in reading, orthographic skills and spelling.

Physical form

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
Marino C
European Journal of Human Genetics, 13, 491-499 (2005)
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK
Psychiatric Genetics, 24, 10-20 (2014)
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins.
Tammimies K
Biological Psychiatry, 73, 583-590 (2013)
Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population.
Zhang Y
PLoS ONE, 7 (2012)
DYX1C1 is required for axonemal dynein assembly and ciliary motility.
Tarkar A
Nature Genetics, 45, 995-995 (2013)

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