NALP12 (NLRP12) (NM_144687) Human 3' UTR Clone
CAT#: SC206277
3' UTR clone of NLR family pyrin domain containing 12 (NLRP12) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | NALP12 (NLRP12) (NM_144687) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2 |
ACCN | NM_144687 |
Insert Size | 338 bp |
Sequence Data |
>SC206277 3’UTR clone of NM_144687
The sequence shown below is from the reference sequence of NM_144687. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACAAAACCTTATTTGGACATTGGCTGCTGAATGGTCCTATCTGCTGGCTCTCCCCTGAGATCTGGACAG AGGAAGATGGGAGGGTGCTCATCACCCCCCCAGCATAATGATCAGCCTCCTTCCTAGAGACAGACTCAT GCAGATTGAGATCAAAAGTCCCTCTGCTTGGGATCAAATTAATGTTTGACAGAGCTGGCCAGGCGTGGT GGCTCATGTATGTAATCCTAGCACTTCGAGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGTTTGAGA TTAGCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAATAAAAAAAAATTAGCCAGGCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_144687.4 |
Synonyms | CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2 |
Summary | This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013] |
Locus ID | 91662 |
MW | 12.6 |
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