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Flag-tagged LOC69864 in pcDNA3.1(+)

Expression vector of FLAG-tagged mouse LOC69864.

Catalog number RDB14270
Resource name Flag-tagged LOC69864 in pcDNA3.1(+)
Clone info. Expression vector of FLAG-tagged mouse LOC69864 (an uncharacterized protein that is structurally most similar to Lypd8).
Expression was confirmed by the depositor with immunostaining.
Vector backbone pcDNA3.1(+) (Plasmid)
Size of vector backbone 5.4 kb
Selectable markers Amp^r (E. coli), Neo^r (mammalian cells).
Gene/insert name mouse LOC69864 cDNA
Depositor Takeda, Kiyoshi |
 
Other clones in our bank mouse 1810065E05Rik (NCBI Gene 69864) |

Distribution information

Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
Terms and conditions set forth by the DEPOSITOR In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature designated by the DEPOSITOR is requested. (Okumura, R. et al., Nature, 532 (7597): 117-121, 2016) RECIPIENT which wants to use the BIOLOGICAL RESOURCE for the purpose other than education or not-for-profit research is requested to enter into a Material Transfer Agreement with Osaka University.
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Catalog # Resource name Availability Shipping form Fee (non-profit org.)
RDB14270 Flag-tagged LOC69864 in pcDNA3.1(+) Under QC test. Please contact us. DNA solution

Ordering Information [in Japanese] [in English]

References and tips

Electronic file

Original reference

original Okumura, R., Lypd8 promotes the segregation of flagellated microbiota and colonic epithelia. Nature 532 (7597): 117-121, (2016). PMID 27027293.

Further references such as user reports and related articles (go to bottom)

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Sequence information

This clone will be sequenced a portion and digested by restriction enzyme for examination.


References

Original, user report and related articles

original Okumura, R., Lypd8 promotes the segregation of flagellated microbiota and colonic epithelia. Nature 532 (7597): 117-121, (2016). PMID 27027293.

2019.07.19

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