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SAB1400075

Anti-DDX11 antibody produced in mouse

IgG fraction of antiserum, buffered aqueous solution

Synonym(s):

Anti-CHL1, Anti-CHLR1, Anti-KRG2, Anti-MGC133249, Anti-MGC9335

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About This Item

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
IF, WB
Citations:
5
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biological source

mouse

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human

technique(s)

indirect immunofluorescence: suitable, western blot: 1 μg/mL

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... DDX11(1663)

General description

DEAD/H-box helicase 11 (DDX11) gene is located on human chromosome 12p11.21. DDX11 encodes an iron sulphur containing DNA helicase. DDX11 is overexpressed in melanomas.

Immunogen

DDX11 (AAH50522.1, 1 a.a. ~ 970 a.a) full-length human protein.

Sequence
MANETQKVGAIHFPFPFTPYSIQEDFMAELYRVLEAGKIGIFESPTGTGKSLSLICGALSWLRDFEQKKREEEARLLETGTGPLHDEKDESLCLSSSCEGAAGTPRPAGEPAWVTQFVQKKEERDLVDRLKAEQARRKQREERLQQLQHRVQLKYAAKRLRQEEEERENLLRLSREMLETGPEAERLEQLESGEEELVLAEYESDEEKKVASRVDEDEDDLEEEHITKIYYCSRTHSQLAQFVHEVKKSPFGKDVRLVSLGSRQNLCVNEDVKSLGSVQLINDRCVDMQRSRHEKKKGAEEEKPKRRRQEKQAACPFYNHEQMGLLRDEALAEVKDMEQLLALGKEARACPYYGSRLAIPAAQLVVLPYQMLLHAATRQAAGIRLQDQVVIIDEAHNLIDTITGMHSVEVSGSQLCQAHSQLLQYVERYGKRLKAKNLMYLKQILYLLEKFVAVLGGNIKQNPNTQSLSQTGTELKTINDFLFQSQIDNINLFKVQRYCEKSMISRKLFGFTERYGAVFSSREQPKLAGFQQFLQSLQPRTTEALAAPADESQASTLRPASPLMHIQGFLAALTMANQDGRVILSRQGSLSQSTLKFLLLNPAVHFAQVVKECRAVVIAGGTMQPVSDFRQQLLACAGVEAERVVEFSCGHVIPPDNILPLVICSGISNQPLEFTFQKRELPQMMDEVGRILCNLCGVVPGGVVCFFPSYEYLRQVHAHWEKGGLLGRLAARKKIFQEPKSAHQVEQVLLAYSRCIQACGQERGQVTGALLLSVVGGKMSEGINFSDNLGRCVVMVGMPFPNIRSAELQEKMAYLDQTLSPRPGTPREGSGGEPVHEGRQPVHRQGHQAPEGFCQRSAPGPAICPAPCPGQAAGLDPSPCGGQSYLWPRHCCCAEVSPGEVGLFLMGNHTTAWRRALPLSCPLETVFVVGVVCGDPVTKVKPRRRVWSPECCQDPGTGVSSRRRKWGNPE

Application

Anti-DDX11 antibody produced in mouse has been used in western blotting.

Biochem/physiol Actions

DEAD/H-box helicase 11 (DDX11) maintains the cohesion of chromosome arms and centromeres. It plays an important role in genomic stability. Downregulation of DDX11 in melanoma cells causes inhibition of melanoma cell proliferation, defective chromosome segregation and apoptosis. DDX11 is required for the formation of heterochromatin. Mutations in this gene is linked to Warsaw breakage syndrome (WABS).

Physical form

Solution in phosphate buffered saline, pH 7.4

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

Regulatory Information

低风险生物材料
常规特殊物品
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Specialization among iron-sulfur cluster helicases to resolve G-quadruplex DNA structures that threaten genomic stability
Bharti SK, et al
The Journal of Biological Chemistry, jbc-M113 (2013)
The DEAD/DEAH box helicase, DDX11, is essential for the survival of advanced melanomas
Bhattacharya C, et al.
Molecular Cancer, 11(1), 82-82 (2012)
Clinical Report: Warsaw Breakage Syndrome with small radii and fibulae
Eppley S, et al.
American Journal of Medical Genetics. Part A, 173(11), 3075-3081 (2017)
Mammalian ChlR1 has a role in heterochromatin organization
Inoue A, et al.
Experimental Cell Research, 317(17), 2522-2535 (2011)
Merlin G Butler et al.
International journal of molecular sciences, 16(3), 6464-6495 (2015-03-25)
Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic

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