RHAG (NM_000324) Human 3' UTR Clone

Specifications

Product Data
Product Name	RHAG (NM_000324) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CD241; OHS; OHST; RH2; Rh50; RH50A; Rh50GP; RHNR; SLC42A1
ACCN	NM_000324
Insert Size	668 bp
Sequence Data	Insert Sequence (showhide) >SC208605 3’UTR clone of NM_000324 The sequence shown below is from the reference sequence of NM_000324. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTTTATTGGAAGGTCCCTAAGACGAGATAACTTGACAATCAGTTCCATGGACATGGTGACCACAGCCAG CTGGAACCTGAAGTCTAAACACCATTCCTGCTCTCCAGCTTCCTTTCCCATTATCCAGAATCAAGTCCA AATAAACAAAAAGGGAGTAACCAAAGAGAGTATGGACCAGAGTGAATAGATCCTAAGTCCCAAATGGCC AGTGTAAAAATGTCCTTATGTCTGATGCTGTCTCTTGCTCTTCAATGATTAATTGAGGGGATGTTACTC ATAAAACAGATAATCAAATAGATCTTCTCCAGGATTCCCAAAAAGCTTTTGGCAGTGAGTAAATACAGA GTAAACATGTCAGTTTCTTAATGTAGACACTATGTCTTCAATCCCAAAAATTATAAAACTGAAACCCAT GAAGCAAGAATAGATGTGAGAAATCTATGTAAAAAAATAATTAAAGAAATGCATGTGTGTAAAGTAGTA ATATGATGATTTTAGGTAGTGCTTTTTATTTTAAAAATAGTCTAGTTAGTAATGTTGTATCCTTGCATG AATATTATTCTTAATTCCTTTTGCATGTTGACTATTTGCAACGAGCTCAAATGCTATCTGATCAAAGTC TATTTTGCATAAAATGTCCAATAATTAAATATTGTTATAAAATAAAA 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_000324.3
Synonyms	CD241; OHS; OHST; RH2; Rh50; RH50A; Rh50GP; RHNR; SLC42A1
Summary	The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009]
Locus ID	6005
MW	25.7

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