RHD (NM_016124) Human Untagged Clone

CAT#: SC111686

RHD (untagged)-Human Rh blood group, D antigen (RHD), transcript variant 1


  "NM_016124" in other vectors (6)

Reconstitution Protocol

USD 710.00

In Stock*

Size
    • 10 ug

Product Images

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol RHD
Synonyms CD240D; DIIIc; RH; Rh4; RH30; RHCED; RhDCw; RHDel; RHDVA(TT); RhII; RhK562-II; RhPI; RHPII; RHXIII
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC111686 sequence for NM_016124 edited (data generated by NextGen Sequencing)
ATGAGCTCTAAGTACCCGCGGTCTGTCCGGCGCTGCCTGCCCCTCTGGGCCCTAACACTG
GAAGCAGCTCTCATTCTCCTCTTCTATTTTTTTACCCACTATGACGCTTCCTTAGAGGAT
CAAAAGGGGCTCGTGGCATCCTATCAAGTTGGCCAAGATCTGACCGTGATGGCGGCCATT
GGCTTGGGCTTCCTCACCTCGAGTTTCCGGAGACACAGCTGGAGCAGTGTGGCCTTCAAC
CTCTTCATGCTGGCGCTTGGTGTGCAGTGGGCAATCCTGCTGGACGGCTTCCTGAGCCAG
TTCCCTTCTGGGAAGGTGGTCATCACACTGTTCAGTATTCGGCTGGCCACCATGAGTGCT
TTGTCGGTGCTGATCTCAGTGGATGCTGTCTTGGGGAAGGTCAACTTGGCGCAGTTGGTG
GTGATGGTGCTGGTGGAGGTGACAGCTTTAGGCAACCTGAGGATGGTCATCAGTAATATC
TTCAACACAGACTACCACATGAACATGATGCACATCTACGTGTTCGCAGCCTATTTTGGG
CTGTCTGTGGCCTGGTGCCTGCCAAAGCCTCTACCCGAGGGAACGGAGGATAAAGATCAG
ACAGCAACGATACCCAGTTTGTCTGCCATGCTGGGCGCCCTCTTCTTGTGGATGTTCTGG
CCAAGTTTCAACTCTGCTCTGCTGAGAAGTCCAATCGAAAGGAAGAATGCCGTGTTCAAC
ACCTACTATGCTGTAGCAGTCAGCGTGGTGACAGCCATCTCAGGGTCATCCTTGGCTCAC
CCCCAAGGGAAGATCAGCAAGACTTATGTGCACAGTGCGGTGTTGGCAGGAGGCGTGGCT
GTGGGTACCTCGTGTCACCTGATCCCTTCTCCGTGGCTTGCCATGGTGCTGGGTCTTGTG
GCTGGGCTGATCTCCGTCGGGGGAGCCAAGTACCTGCCGGGGTGTTGTAACCGAGTGCTG
GGGATTCCCCACAGCTCCATCATGGGCTACAACTTCAGCTTGCTGGGTCTGCTTGGAGAG
ATCATCTACATTGTGCTGCTGGTGCTTGATACCGTCGGAGCCGGCAATGGCATGATTGGC
TTCCAGGTCCTCCTCAGCATTGGGGAACTCAGCTTGGCCATCGTGATAGCTCTCACGTCT
GGTCTCCTGACAGGTTTGCTCCTAAATCTTAAAATATGGAAAGCACCTCATGAGGCTAAA
TATTTTGATGACCAAGTTTTCTGGAAGTTTCCTCATTTGGCTGTTGGATTTTAA

Clone variation with respect to NM_016124.3
>OriGene 5' read for NM_016124 unedited
GCATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGCTGGTGCTGGT
GGAACCCCTGCACAGAGACGGACACAGGATGAGCTCTAAGTACCCGCGGTCTGTCCGGCG
CTGCCTGCCCCTCTGGGCCCTAACACTGGAAGCAGCTCTCATTCTCCTCTTCTATTTTTT
TACCCACTATGACGCTTCCTTAGAGGATCAAAAGGGGCTCGTGGCATCCTATCAAGTTGG
CCAAGATCTGACCGTGATGGCGGCCATTGGCTTGGGCTTCCTCACCTCGAGTTTCCGGAG
ACACAGCTGGAGCAGTGTGGCCTTCAACCTCTTCATGCTGGCGCTTGGTGTGCAGTGGGC
AATCCTGCTGGACGGCTTCCTGAGCCAGTTCCCTTCTGGGAAGGTGGTCATCACACTGTT
CAGTATTCGGCTGGCCACCATGAGTGCTTTGTCGGTGCTGATCTCAGTGGATGCTGTCTT
GGGGAAGGTCAACTTGGCGCAGTTGGTGGTGATGGTGCTGGTGGAGGTGACAGCTTTAGG
CAACCTGAGGATGGTCATCAGTAATATCTTCAACACAGACTACCACATGAACATGATGCA
CATCTACGTGTTCGCAGCCTATTTTGGGCTGTCTGTGGCCTGGTGCCTGCCAAAGCCTCT
ACCCGAGGGAACGGAGGATAAAGATCAGACAGCAACGATACCCAGTTTGTCTGCCATGCT
GGGCGCCCTCTTCTTGTGGATGTTCTGGCCAAGTTTCAACTCTGCTCTGCTGAGAAGTCC
AATCGAAGGGAGAATGCCGTGTTCACACCTACTATGCTGTAGCAGTCAGCGTGGTGACAG
CCATCTCAGGGTCATCCTTGGCTCACCCNCAGGGNAAGATCAGCAGACTATGTGCACAGT
GCGTGTTGGCAAGAGCGTGGCTGTGGNTACCTCGTGTCACCTGATCCCTTCTNCGTGGCT
NGCCATGGNGCTGGGN
>OriGene 3' read for NM_016124 unedited
AAACAAGGAAAACACCANACACATTCCCCCCCCCTTTTTACTTGNNACGCGGCCGCATTT
NANGATCGGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTT
TTTTTTTTTTTATGGGGAACATGGCTGTATTTTATTGGTGAATTCTACAGCGCATAAAAA
ATGGGGAAATTTTCCTCAAAAAGGGCAAAAAAAGGATTCAACTCCATTTTCTTTGACTCC
AGGGCCTGGGCAAACATTGGAAACTTTGCTGTCATAAGCGTTTCTCACCTCCAAATGCCG
GCAACAGTGAAAGGAATTTGTCTTGTTTTTAAACAGGCCTTGTTTTTTTTGGATGCTTTT
GCTTAAAATCCAACCTCCAAATGAGGAAACTTCCAAAAAACTTGGTCCTCAAAATATTTA
ACCTCATGAGGGGCTTTCCATTTTTTAAAATTTAGGAACAAACCTGTCCGGAGACCAAAC
GTGAAATCTTTCACCACGGCCAAGCTGATTTCCCCAATGTTGGGGAGGCCCTTGAAACCA
ATCCTGCCATTGGCCGGCTCCAACGGGTTCAAACACCCCCCCAACAATGTAACAAATCTT
CTCAAGCACAACCAACAGGTTCAACTTGAACCCCTTTATGGAACCCGCGGGGGAAATCCC
CCGATTTTGGTTCCAAAACCCCCGGAGAGACTTTGGGTTCCCCCGCGGGAAATTCCCCCC
ACCCCAAACACCCACCCCCTTGGCCACCCCCCCGTAAAAGGTGACCGGTTACAACAAGTA
TCCTCCCAGGTCCCCTTTTTTGGAAAACCCGATTTGTGAAAAAAAAGCCTGGTGGAATTT
CCCTGGGGGGGAGCCACACGGAATCCTCTTAAATGGGTTTACCCACTCTATTTGTTAAAA
TTAATAGGGGTTTAAACACGGCTTTTTCTTTTCTCATGGACCCCCCCCACAAAAATAATT
CAACCCTGGCCAAAATCCCCCACTAAACGGG
Restriction Sites NotI-NotI     
ACCN NM_016124
Insert Size 1550 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 cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
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_016124.2, NP_057208.2
RefSeq Size 2709 bp
RefSeq ORF 1254 bp
Locus ID 6007
Cytogenetics 1p36.11
Domains Ammonium_transp
Protein Families Transmembrane
Gene Summary 'The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene, which encodes the RhD protein, and a second gene that encodes both the RhC and RhE antigens on a single polypeptide. The two genes, and a third unrelated gene, are found in a cluster on chromosome 1. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]'
Transcript Variant: This variant (1) represents the predominant transcript and encodes isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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