CD3D (NM_001040651) Human 3' UTR Clone
CAT#: SC200889
3' UTR clone of CD3d molecule delta (CD3-TCR complex) (CD3D) transcript variant 2 for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CN¥ 4,845.00
货期*
3周
规格
Product images

经常一起买 (2)
Specifications
Product Data | |
Product Name | CD3D (NM_001040651) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CD3-DELTA; IMD19; T3D |
ACCN | NM_001040651 |
Insert Size | 238 bp |
Sequence Data |
>SC200889 3’UTR clone of NM_001040651
The sequence shown below is from the reference sequence of NM_001040651. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTGGAGGAAACTGGGCTCGGAACAAGTGAACCTGAGACTGGTGGCTTCTAGAAGCAGCCATTACCAAC TGTACCTTCCCTTCTTGCTCAGCCAATAAATATATCCTCTTTCACTCAGCAGGTGCCTGGGCTTCTTAA GGCTCCTGGGCAAGGCGTGGGAGTTGTCCTGACTTGCTTGGGATCTCGCCCTCCTACCTACCTGTTTCT TCCTTCATCTCCTTCCTTCCTCTGCCTCACA 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_001040651.2 |
Synonyms | CD3-DELTA; IMD19; T3D |
Summary | The protein encoded by this gene is part of the T-cell receptor/CD3 complex (TCR/CD3 complex) and is involved in T-cell development and signal transduction. The encoded membrane protein represents the delta subunit of the CD3 complex, and along with four other CD3 subunits, binds either TCR alpha/beta or TCR gamma/delta to form the TCR/CD3 complex on the surface of T-cells. Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK). Two transcript variants encoding different isoforms have been found for this gene. Other variants may also exist, but the full-length natures of their transcripts has yet to be defined. [provided by RefSeq, Feb 2009] |
Locus ID | 915 |
MW | 8.7 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...