C1orf2 (FAM189B) (NM_198264) Human 3' UTR Clone

CAT#: SC207895

3`UTR clone of family with sequence similarity 189 member B (FAM189B) transcript variant 2 for miRNA target validation


Reconstitution Protocol

USD 560.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol FAM189B
Synonyms C1orf2; COTE1
ACCN NM_198264
Insert Size 566
Sequence Data
>SC207895 3'UTR clone of NM_198264
The sequence shown below is from the reference sequence of NM_198264. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

GGGAGACTGGGCTCTGACCTAGGCTTCTTGTCACACTGAACACATCCAGCCACAGGCACCAGCTGGTTGG
GACCAGCAGCCCCCAGCATCCTCTTGCACTGGCTGGCACAAAAAGAAACCTGCTGTATACCCCCCAAAGT
GTCCCTTTCCCTCCTACCTCTGGGGTCTCTTGCTGCTTGCCTCTGCTGCTCTGGACTGGGAGAGCTTCTG
TCCTGTGCTGCATGGGTATTTAGACTGTGGGGGAGATGCCCCTTCTTATAGCACTGGAGGAGGAAAACAA
ATTCTTGTCCCCCTCAGAATGAGAGTGGCTCTTTCTGATTTGCAAGGGCACTATGGTCAGGGCAAAGGCA
TGGCCCAGGTGTTTAAGTACAGGGTGACGTGTGCCTATGCAATGGGGTGGTAAGGCAGGCACGAAGAGTC
CAAAAAATCTAGGTGGCCTCTCAGCTCTGCCACCTCTAGCTGCATGACCTTGGGCAAGCTATGTAACCCC
AATTGCCTGCTCCATTAAAGACTGTGAAGGTAGAATGTTTGTAAAGCTCTTAACAGTATGTAAGCCTTCA
ATAAAT

ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_198264.1
Summary This gene is located near the gene for the lysosomal enzyme glucosylceramidase; a deficiency in this enzyme is associated with Gaucher disease. The encoded protein has been identified as a potential binding partner of a WW domain-containing protein which is involved in apoptosis and tumor suppression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
Locus ID 10712

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