GDNF Receptor alpha 1 (GFRA1) (NM_005264) Human Untagged Clone

CAT#: SC127971

GFRA1 (untagged)-Human GDNF family receptor alpha 1 (GFRA1), transcript variant 1


  "NM_005264" in other vectors (6)

Reconstitution Protocol

USD 457.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol GDNF Receptor alpha 1
Synonyms GDNFR; GDNFRA; GFR-ALPHA-1; GFRalpha-1; RET1L; RETL1; TRNR1
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC127971 sequence for NM_005264 edited (data generated by NextGen Sequencing)
ATGTTCCTGGCGACCCTGTACTTCGCGCTGCCGCTCTTGGACTTGCTCCTGTCGGCCGAA
GTGAGCGGCGGAGACCGCCTGGATTGCGTGAAAGCCAGTGATCAGTGCCTGAAGGAGCAG
AGCTGCAGCACCAAGTACCGCACGCTAAGGCAGTGCGTGGCGGGCAAGGAGACCAACTTC
AGCCTGGCATCCGGCCTGGAGGCCAAGGATGAGTGCCGCAGCGCCATGGAGGCCCTGAAG
CAGAAGTCGCTCTACAACTGCCGCTGCAAGCGGGGTATGAAGAAGGAGAAGAACTGCCTG
CGCATTTACTGGAGCATGTACCAGAGCCTGCAGGGAAATGATCTGCTGGAGGATTCCCCA
TATGAACCAGTTAACAGCAGATTGTCAGATATATTCCGGGTGGTCCCATTCATATCAGAT
GTTTTTCAGCAAGTGGAGCACATTCCCAAAGGGAACAACTGCCTGGATGCAGCGAAGGCC
TGCAACCTCGACGACATTTGCAAGAAGTACAGGTCGGCGTACATCACCCCGTGCACCACC
AGCGTGTCCAACGATGTCTGCAACCGCCGCAAGTGCCACAAGGCCCTCCGGCAGTTCTTT
GACAAGGTCCCGGCCAAGCACAGCTACGGAATGCTCTTCTGCTCCTGCCGGGACATCGCC
TGCACAGAGCGGAGGCGACAGACCATCGTGCCTGTGTGCTCCTATGAAGAGAGGGAGAAG
CCCAACTGTTTGAATTTGCAGGACTCCTGCAAGACGAATTACATCTGCAGATCTCGCCTT
GCGGATTTTTTTACCAACTGCCAGCCAGAGTCAAGGTCTGTCAGCAGCTGTCTAAAGGAA
AACTACGCTGACTGCCTCCTCGCCTACTCGGGGCTTATTGGCACAGTCATGACCCCCAAC
TACATAGACTCCAGTAGCCTCAGTGTGGCCCCATGGTGTGACTGCAGCAACAGTGGGAAC
GACCTAGAAGAGTGCTTGAAATTTTTGAATTTCTTCAAGGACAATACATGTCTTAAAAAT
GCAATTCAAGCCTTTGGCAATGGCTCCGATGTGACCGTGTGGCAGCCAGCCTTCCCAGTA
CAGACCACCACTGCCACTACCACCACTGCCCTCCGGGTTAAGAACAAGCCCCTGGGGCCA
GCAGGGTCTGAGAATGAAATTCCCACTCATGTTTTGCCACCGTGTGCAAATTTACAGGCA
CAGAAGCTGAAATCCAATGTGTCGGGCAATACACACCTCTGTATTTCCAATGGTAATTAT
GAAAAAGAAGGTCTCGGTGCTTCCAGCCACATAACCACAAAATCAATGGCTGCTCCTCCA
AGCTGTGGTCTGAGCCCACTGCTGGTCCTGGTGGTAACCGCTCTGTCCACCCTATTATCT
TTAACAGAAACATCATAG

Clone variation with respect to NM_005264.4
>OriGene 5' read for NM_005264 unedited
NNNNNGGGGAAGTTCAAAATTGTAATAGACTCATATAGGCGGCCGCGAAATTCGCACGAG
GGATAAAGTGAGCCCGGAAAGNGAAGAGGGGGCGGGGACACCATNNTGCCCTGAAANAAT
AAATAAGTAAATAAACAAACTGGCTCCTCGCCGCAGCTGGACGCGGTCGGTTGAGTCCAG
GTTGGGTCGGACCTGAACCCCTAAAAGCGGAACCGCCTCCCGCCCTCGCCATCCCGGAGC
TGAGTCGCCGGCGGCGGTGGCTGCTGCCAGACCCGGAGTTTCCTCTTTCACTGGATGGAG
CTGAACTTTGGGCGGCCAGAGCAGCACAGCTGTCCGGGGATCGCTGCATGCTGAGCTCCC
TCGGCAAGACCCAGCGGCGGCTCGGGATTTTTTTNGGGGGGGCGGGGACCAGCCCCGCGC
CGGCACCATGTTCCTGGCGACCCTGTACTTCGCGCTGCCGCTCTTGGACTTGCTCCTGTC
GGCCGAAGTGAGCGGCGGAGACCGCCTGGATTGCGTGAAAGCCAGTGATCAGTGCCTGAA
GGAGCAGAGCTGCAGCACCAAGTACCGCACGCTAAGGCAGTGCGTGGCGGGCAAGGAGAC
CAACTTCAGCCTGGCATCCGGCCTGGAGGCCAAGGATGAGTGCCGCAGCGCCATGGAGGC
CCTGAAGCAGAAGTCGCTCTACAACTGCCGCTGCAAGCGGNGTATGAAGAAAGAGAAGAA
CTGCCTGCGCATTTACTGGAGCATGTACCAGAGCCTGCAGGGAAATGATCTGCTGGAGGA
TTCCCCATATGAACCAGTTAACAGCAGATTGTCAGATATATTCCGGGT
>OriGene 3' read for NM_005264 unedited
ATGGACCATGGATGATGGCACTTCCAGGNCCAGNANAGCACTGGGGNAGGGTCACAGGGC
ATGCCACCCGGGCTCTGTTCAGGAAACAGCTATGACCGCGGCCGCAATCTAGAGTCGAGT
TTTTTTTTTTTTTTTTTCTTTTTACATGTCCATATTGTATTTTTTTAATGCAGCTATGAT
GTTTCTGTTAAAGATAATAGGGTGGACAGAGCGGTTACCACCAGGACCAGCAGTGGGCTC
AGACCACAGCTTGGAGGAGCAGCCATTGATTTTGTGGTTATGTGGCTGGAAGCACCGAGA
CCTTCTTTTTCATAATTACCATTGGAAATACAGAGGTGTGTATTGCCCGACACATTGGAT
TTCAGCTTCTGTGCCTGTAAATTTGCACACGGTGGCAAAACATGAGTGGGAATTTCATTC
TCAGACCCTGCTGGCCCCAGGGGCTTGTTCTTAACCCGGAGGGCAGTGGTGGTAGTGGCA
GTGGTGGTCTGTACTGGGAAGGCTGGCTGCCACACGGTCACATCGGAGCCATTGCCAAAG
GCTTGAATTGCATTTTTAAGACATGTATTGTCCTTGAAGAAATTCAAAAATTTCAAGCAC
TCTTCTAGGTCGTTCCCACTGTTGCTGCAGTCACACCATGGGGCCACACTGAGGCTACTG
GAGTCTATGTAGTTGGGGGTCATGACTGTGCCAATAAGCCCCGAGTAGGCGAGGAGGCAG
TCAGCGTAGTTTTCCTTTAAACAGCTGCTGACAGACCTTGACTCTGGCTGGCAGTTGGTA
AAAAAATCCGCAGGCGAGATCTGCAGATGTAATTCGTCTTGCAGGAGTCCTGCCAATCCA
AACAGTTGGGCTTCTCCCTCTCTTCTAGGAGCCCACGGCACGAC
Restriction Sites Please inquire     
ACCN NM_005264
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_005264.2, NP_005255.1
RefSeq Size 2542 bp
RefSeq ORF 1398 bp
Locus ID 2674
UniProt ID P56159
Cytogenetics 10q25.3
Domains GDNF
Protein Families Druggable Genome
Gene Summary This gene encodes a member of the glial cell line-derived neurotrophic factor receptor (GDNFR) family of proteins. The encoded preproprotein is proteolytically processed to generate the mature receptor. Glial cell line-derived neurotrophic factor (GDNF) and neurturin (NTN) are two structurally related, potent neurotrophic factors that play key roles in the control of neuron survival and differentiation. This receptor is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor. This gene is a candidate gene for Hirschsprung disease. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]
Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a). Variants 1 and 6 both encode the same isoform (a). 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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