SCNN1B (NM_000336) Human 3' UTR Clone
CAT#: SC206720
3' UTR clone of sodium channel nonvoltage-gated 1 beta (SCNN1B) 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 | SCNN1B (NM_000336) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BESC1; ENaCb; ENaCbeta; LIDLS1; SCNEB |
ACCN | NM_000336 |
Insert Size | 523 bp |
Sequence Data |
>SC206720 3’UTR clone of NM_000336
The sequence shown below is from the reference sequence of NM_000336. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGTCTGACAGTGAGGGTGATGCCATCTAACCCTGCCCCTGCCCACCCCGGGCGGCTGAAACTCACTGA GCAGCCAAGACTGTTGCCCGAGGCCTCACTGTATGGTGCCCTCTCCAAAGGGTCGGGAGGGTAGCTCTC CAGGCCAGAGCTTGTGTCCTTCAACAGAGAGGCCAGCGGCAACTGGTCCGTTACTGGCCAAGGGCTCTG TAGAATCACGGTGCTGGTACAGGATGCAGGAATAAATTGTATCTTCACCTGGTTCCTACCCTCGTCCCT ACCTGTCCTGATCCTGGTCCTGAAGACCCCTCGGAACACCCTCTCCTGGTGGCAGGCCACTTCCCTCCC AGTGCCAGTCTCCATCCACCCCAGAGAGGAACAGGCGGGTGGGCCATGTGGTTTTCTCCTTCCTGGCCT TGGCTGGCCTCTGGGGCAGGGGTGGTGGAGAGATGGAAGGGCATCAGGTGTAGGGACCCTGCCAAGTGG CACCTGATTTACTCTAGAAAATAAAAGTAGAAAATACTGA 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_000336.3 |
Synonyms | BESC1; ENaCb; ENaCbeta; LIDLS1; SCNEB |
Summary | Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009] |
Locus ID | 6338 |
MW | 19.3 |
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