CFHL2 (CFHR2) (NM_005666) Human 3' UTR Clone
CAT#: SC201447
3' UTR clone of complement factor H-related 2 (CFHR2) for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4845.00
货期*
3周
规格
Product images

推荐一起购买 (2)
Specifications
Product Data | |
Product Name | CFHL2 (CFHR2) (NM_005666) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CFHL2; FHR2; HFL3 |
ACCN | NM_005666 |
Insert Size | 572 bp |
Sequence Data |
>SC201447 3’UTR clone of NM_005666
The sequence shown below is from the reference sequence of NM_005666. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGGTATATCCCAGTTGTGAAGAAAAATAGAATCAATGGCATTACTATTAGTAAAATGCACACCTTTTT CTGAATTTACTATTATATTTGTTTTCAATTTCATTTTTCAAGTACTGTTTTACTCATTTTTATTCATAA ATAAAGTTTTGTGTTGATTTGTGAAAATGCAATTACAATCTGAGATGTGTCACAATGGTGAGGACTATC TTCACCAAATCTAAGTAACAACCTAGGAATTGTCTTTTTTTTTCTTTTTAAAAAAATTGACAATAACTG TATATATTCATGGAGTACATAGTAATGTTTCCATATATATAATGTATAATGGTCAGTTAGGGTAATTAG TATATCCATTATCTCAAACATTTTTCATTTCTTTGGGTTAGGAGCATTAAATATTCTCCTTCCAGCTAT TTGGTACTTCATAGTATATTACTGGTAACTGAAGGAATTATATCTAGACGTTACCCCAGGTATCTTGAA ATGTCAATTCCTAACAGTCACAGCCTGGGAGCTCATGTTTGCCTTCTTTCAGAGCTTGTAACTATGTAT ATCCACATAAATAATCAAAA 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_005666.4 |
Synonyms | CFHL2; FHR2; HFL3 |
Summary | This gene belongs to a family of complement factor H-related genes (CFHR), which are clustered together with complement factor H gene on chromosome 1, and are involved in regulation of complement. Mutations in CFHR genes have been associated with dense deposit disease and atypical haemolytic-uraemic syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015] |
Locus ID | 3080 |
MW | 22.9 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...