DGCR2 (NM_005137) Human Untagged Clone

CAT#: SC116951

DGCR2 (untagged)-Human DiGeorge syndrome critical region gene 2 (DGCR2), transcript variant 1



  "NM_005137" in other vectors (4)

CNY 4,104.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (4)
Rabbit Polyclonal Anti-DGCR2 Antibody
    • 50 ug

CNY 5,250.00


TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Synonyms DGS-C; IDD; LAN; SEZ-12
Vector pCMV6-XL6
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC116951 sequence for NM_005137 edited (data generated by NextGen Sequencing)
ATGGTGCCCAAGGCAGACAGCGGCGCCTTCCTGCTGCTCTTCCTGCTCGTGCTCACTGTC
ACCGAGCCGCTGCGGCCAGAGCTGCGGTGCAACCCTGGGCAGTTTGCGTGTCGCAGCGGC
ACCATCCAGTGCATCCCCCTCCCCTGGCAGTGTGACGGCTGGGCGACTTGCGAGGATGAG
AGCGACGAAGCCAACTGTCCAGAAGTGACCGGGGAGGTGCGTCCTCATCATGGGAAGGAG
GCTGTGGATCCGCGGCAGGGGCGGGCCAGAGGAGGCGACCCTTCGCACTTCCACGCGGTG
AACGTGGCGCAGCCCGTTCGCTTCAGCAGTTTCCTAGGGAAGTGCCCGACAGGGTGGCAC
CACTACGAAGGCACGGCCAGCTGCTACCGGGTCTACCTGAGCGGGGAGAACTACTGGGAT
GCCGCGCAGACCTGCCAGCGCCTGAATGGCTCTCTCGCCACCTTCTCCACTGACCAGGAG
CTGCGCTTTGTCCTGGCCCAGGAATGGGACCAGCCCGAGCGGAGCTTTGGTTGGAAGGAC
CAGCGCAAGTTGTGGGTTGGCTATCAGTATGTTATCACTGGCCGGAACCGCTCCTTGGAA
GGTCGCTGGGAGGTGGCATTCAAAGGCTCTTCAGAGGTGTTCCTGCCCCCAGACCCCATC
TTTGCCTCGGCCATGTCTGAGAACGACAACGTGTTCTGTGCCCAGCTTCAGTGCTTCCAT
TTCCCCACCCTGCGGCACCACGACCTCCACAGCTGGCACGCCGAGAGCTGCTACGAGAAG
TCTTCATTTCTGTGTAAAAGAAGTCAAACATGTGTTGACATCAAGGACAACGTGGTGGAT
GAAGGGTTCTACTTCACCCCTAAGGGGGACGACCCATGCCTGAGCTGCACCTGCCATGGA
GGGGAGCCTGAGATGTGTGTGGCTGCTCTCTGTGAGAGGCCCCAGGGCTGCCAACAGTAC
CGCAAGGACCCCAAAGAGTGCTGCAAGTTCATGTGTCTGGACCCAGATGGCAACAGTCTG
TTTGACTCCATGGCCAGCGGGATGCGCCTGGTCGTCAGCTGCATCTCCTCCTTCCTCATC
CTGTCACTGCTGCTCTTCATGGTCCACCGGCTGCGCCAGCGGCGCCGGGAGCGCATCGAG
TCCCTGATTGGAGCAAACTTGCACCACTTCAACCTCGGCCGCAGGATCCCTGGCTTTGAT
TACGGCCCAGACGGGTTTGGCACGGGCCTCACGCCGCTGCATCTTTCTGACGACGGAGAG
GGTGGGACTTTCCATTTCCACGACCCTCCACCTCCCTACACGGCATACAAGTACCCGGAC
ATCGGCCAGCCCGACGACCCTCCGCCGCCCTACGAGGCCTCCATCCACCCGGACAGTGTG
TTCTATGACCCTGCAGACGATGATGCTTTTGAGCCTGTGGAGGTCAGCCTGCCAGCCCCT
GGGGATGGTGGGAGTGAAGGTGCATTACTCCGGCGCCTGGAGCAGCCTCTGCCCACTGCG
GGGGCCTCTCTGGCAGACCTGGAAGACTCTGCCGACAGCAGCAGCGCCCTGCTCGTGCCC
CCTGACCCTGCCCAGAGCGGGAGCACCCCAGCTGCAGAGGCACTGCCAGGGGGTGGCCGC
CACAGCCGCAGCTCCCTCAATACTGTGGTGTAG

Clone variation with respect to NM_005137.2
>OriGene 5' read for NM_005137 unedited
GTCTATCACCCGCCCCGTTGNACGCAAATGGGCGGTAGGCGTGTACGGTGGGAGGTCTAT
ATAAGCAGAGCTCATTTAGGTGACACTATAGAATACAAGCTACTTGTTCTTTTTGCAGCG
GCCGCGAATTCGGCACGAGGCTGGAGTCGGTGCCTGAGGTTGCAGCCGAGAGTGTGCGCC
AGCCCGCGGCCCAGCCGAAGCTCTTTCCCGCCGCCTCTCCGCGCCTCGCCCAGGTTCAGC
TCCGCCTGACCCTCCGCTTGGCACGGTCCCCTGACCCTCAGTCCGGCCTGGTCCGGCCTT
CCAGCCGCCCCGGGGACGATGAACGGAGGATAAATGGTGCCCAAGGCAGACAGCGGCGCC
TTCCTGCTGCTCTTCCTGCTCGTGCTCACTGTCACCGAGCCGCTGCGGCCAGAGCTGCGG
TGCAACCCTGGGCAGTTTGCGTGTCGCAGCGGCACCATCCAGTGCATCCCCCTCCCCTGG
CAGTGTGACGGCTGGGCGACTTGCGAGGATGAGAGCGACGAAGCCAACTGTCCAGAAGTG
ACCGGGGAGGTGCGTCCTCATCATGGGAAGGAGGCTGTGGATCCGCGGCAGGGGCGGGCC
AGAGGAGGCGACCCTTCGCACTTCCACGCGGTGAACGTGGCGCAGCCCGTTCGCTTCAGC
AGTTTCCTAGGGAAGTGCCCGACAGGGTGGCACCACTACGAAGGCACGGCCAGCTGCTAC
CGGGTCTACCTGAGCGGNGAGAACTACTGGGATGCCGCGCAGACCTGCCAGCGCCTGAAT
GGCTCTCTCGCCACCTTCTCCACTGACCAGGAGCTGCGCTTTGTCCTGGCCCAGGATGGG
ACCAGCCCGAGCGGAGCTTTGGTTGGAAGGACCAGCGCAAGTTGTGGGTTGGCTATCAGT
ATGTTATCACA
>OriGene 3' read for NM_005137 unedited
TTTTGGGTATACTATGNACCGCGCCGCATTCTANNGATCGATTTTTTTTTTTTTTTTTTC
CGGAACACAGTTTATTTGGCATTTGGATGAAATGATTCTCACAGCATCTTAAGAAAATTA
GTGTCAACCCAACCAAAAACTAAAAACCCTTAATGAAAACATAAAAAAACAGGCATCAAG
ACAATGTACAGTATCAAATCCCACCTCCGCATGGCAGGTCAGAGGGCACCTGGGCTCTGA
GAAACCGTGGCAAGCTGGTCCTAGAGGAGGAGGACCCCTGGAGCACAAGGTTCAGCAAGG
GTGACCCCGGGACTTGCTGGTCAGACTGGGGACTGCAGCAGGCCTTGCAAAGGGGGCATT
CTGGATGGTGGTGCAAGAACAGATGAGCGAGTCCAGCTCTCCTCATGCTCCCAAGGGCCT
CCTGGAGCCACAGTGGCAGCGGTGTTCCAGGCAGCCCTGCCATGTGGACCTTCTGCCTGG
CCCAACGTGCCAGTGGCCTGAGTGCTTGTGGAGGCCCATGGGGAAGGGGCCACCCAGCAA
CCCCGGCCAGCCCAAGGCCCACCCTCTGCAGCCTGCATGGTCCACTTTACCCCGTTTCCT
CACTGCCCCCTACGTGTCTGACCGGCCCCTAATGTTCCTCTGGTCCCCAAAGGAAGCGTC
CCAGTCCCACACATCTCGTGCCAGCCACCCTGTCCCGCACACACAGTTCTGAGGCCTGGC
AGGAATCCTCTGAGCTCTCAGGCTCAAGCCCGTGGGGGACTCTGCTGCGTGGTCCTCGGG
CCCTCACTGGCCACCTGGCACCCATAATGCACATGCCTGCTGCTCTGGAAACTGGCTGCC
CTGCCCCAATGCATGTGGGGATCCACGGCATGCTTCCTGGCTTGGCCTCTA
Restriction Sites NotI-NotI     
ACCN NM_005137
Insert Size 4500 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_005137.1, NP_005128.1
RefSeq Size 4436 bp
RefSeq ORF 1653 bp
Locus ID 9993
UniProt ID P98153
Domains VWC, CLECT, ldl_recept_a
Protein Families Druggable Genome, Transmembrane
Gene Summary Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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