RASAL1 (NM_004658) Human Untagged Clone

CAT#: SC122686

RASAL1 (untagged)-Human RAS protein activator like 1 (GAP1 like) (RASAL1), transcript variant 2


  "NM_004658" in other vectors (6)

Reconstitution Protocol

USD 760.00

2 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol RASAL1
Synonyms RASAL
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene sequence for NM_004658 edited
CCCCGGGCACCTACACCTTCTCCTCTTTCGGAAATCTCCCATCCAGCTACCCGGGTCTCG
GACAGGCGGCACTGGGACCACGAGGCAGGGAGCCAGGCTTGAAGCAGGTGACATGTAGAC
GTCCCCTGGTCCAGCCTCGGAACCTGAGCGCCCTTCTGCCTGGAAAGTTTGTGGCTAGGC
GCCATGGCCAAGAGCAGCTCCCTGAATGTTCGCGTGGTGGAGGGCCGCGCGCTGCCTGCC
AAGGACGTGTCTGGGAGCAGCGACCCCTACTGCCTAGTGAAAGTGGACGACGAGGTGGTG
GCCAGGACAGCTACTGTCTGGAGGAGCCTGGGCCCCTTCTGGGGGGAGGAGTACACGGTG
CACCTGCCTCTGGATTTCCACCAGCTGGCCTTCTACGTGCTGGATGAGGACACTGTCGGG
CACGACGACATCATCGGCAAGATCTCGCTGAGCAGGGAGGCGATTACAGCCGACCCCCGA
GGGATTGACAGCTGGATTAACTTGAGCCGAGTGGACCCAGATGCAGAAGTGCAGGGTGAG
ATCTGCCTGTCAGTGCAGATGCTGGAGGATGGGCAGGGCCGCTGCCTTCGCTGCCATGTG
CTTCAGGCCAGGGACCTGGCTCCCAGAGACATCTCTGGCACATCTGACCCATTTGCACGT
GTGTTTTGGGGCAGCCAGAGCTTGGAGACCTCAACCATCAAGAAGACTCGCTTCCCGCAC
TGGGATGAAGTGCTGGAGCTGCGGGAGATGCCAGGTGCCCCGTCCCCACTGCGGGTGGAG
CTCTGGGACTGGGACATGGTGGGCAAGAATGACTTCTTGGGCATGGTGGAGTTCTCTCCA
AAGACCCTCCAGCAGAAGCCACCTAAAGGCTGGTTCCGCCTCCTGCCCTTTCCCAGAGCC
GAGGAGGATTCTGGGGGGAACCTGGGTGCCCTGCGAGTGAAGGTACGCCTGATTGAGGAC
CGCGTCCTGCCCTCCCAGTGCTACCAGCCTCTCATGGAGCTGCTCATGGAGTCTGTGCAG
GGGCCAGCAGAGGAGGACACTGCTAGCCCCTTGGCTTTGCTGGAAGAGCTGACCTTGGGG
GACTGCCGCCAGGACCTTGCCACCAAGCTGGTGAAACTCTTTCTTGGCCGGGGACTGGCT
GGGCACTTTCTGGACTATCTCACCCGGCGTGAGGTGGCTCGGACCATGGACCCCAACACC
CTCTTCCGTTCTAACTCCCTGGCATCCAAGTCGATGGAACAGTTTATGAAGCTCGTGGGC
ATGCCCTACCTGCACGAGGTCCTGAAGCCTGTGATTAGCCGTGTCTTTGAGGAGAAGAAG
TACATGGAGCTGGATCCCTGCAAGATGGACCTGGGCCGCACCCGGAGGATCTCCTTCAAA
GGCGCACTCTCGGAGGAGCAGATGCGGGAGACCAGCCTGGGGCTGCTGACGGGCTACCTG
GGGCCCATCGTGGACGCCATCGTGGGCTCCGTGGGGCGCTGCCCGCCCGCCATGCGCCTC
GCCTTCAAGCAGCTGCACCGGCGAGTGGAGGAGCGCTTCCCCCAGGCCGAGCACCAGGAT
GTGAAGTACCTGGCCATCAGTGGATTTCTCTTCTTGCGATTCTTCGCACCTGCCATCCTT
ACCCCAAAGCTGTTTGACCTTCGGGACCAACACGCGGACCCCCAGACTAGCCGCTCACTG
CTGTTGCTTGCCAAGGCTGTGCAGAGCATTGGAAACCTGGGCCAGCAGCTGGGCCAAGGC
AAGGAACTGTGGATGGCCCCCCTGCACCCCTTCCTGCTGCAGTGTGTCTCACGTGTGAGA
GACTTCCTGGACCGGCTGGTGGATGTGGATGGGGATGAAGCTGGTGTCCCAGCCAGGGCC
CTGTTCCCGCCCTCGGCCATTGTTCGAGAAGGCTATCTGCTGAAGCGCAAGGAGGAGCCT
GCCGGCCTGGCCACGCGCTTTGCCTTCAAGAAGCGCTACGTCTGGCTCAGCGGGGAGACC
CTCTCCTTCTCCAAGAGTCCTGAGTGGCAGGTGGTGACGCAGGACGGCACGGGGGCGCTG
CACACCACCTACCTCCAGTGCAAGAATGTGAATGAGCTCAACCAGTGGCTCTCGGCCTTG
CGCAAGGCCAGCGCCCCCAACCCGAACAAGCTGGCCGCCTGCCACCCCGGTGCCTTCCGC
AGCGCGCGCTGGACCTGCTGCCTCCAGGCTGAGCGCTCAGCCGCCGGCTGCAGCCGTACA
CACTCAGCTGTCACCCTGGGGGACTGGAGTGACCCACTGGATCCTGATGCTGAGGCCCAG
ACAGTGTATCGGCAGCTGCTCCTGGGGCGGGACCAGCTCAGGCTGAAATTACTGGAGGAT
TCTAACATGGATACAACTCTGGAGGCAGACACAGGGGCCTGTCCTGAGGTCCTGGCCCGG
CAAAGAGCAGCAACTGCCCGCCTGCTGGAGGTGCTCGCAGACCTGGATCGTGCCCACGAG
GAGTTCCAGCAGCAGGAGCGAGGGAAGGCGGCCCTGGGCCCCCTTGGCCCCTAAGGAAAT
GCCAGAGCTAGCCCGGAAGGAGGAGCAAGAGCCAGGGGGCCCTCTTCAGCGCATCCTGCC
CCGGGAGTCTCCTGTCTCCTTGGACCTCTTTGATTCTGTGGTTTGGAGGCTCCCAGAGAC
GTGCCTAGTCCTGTGTGCCTTGAGTCCAGAACTCAGGGCATGGAAGCCCTTTGGCAGGGG
CCAGCCTTGCACTGAGTGAAACTTGCCCTCTGGCTTGATTCAGACTGGAGTGGATAGGAT
AAGGAACCTGACTTATTTGACTGAGACTGGGGTCTCTACTTCACCAAACTGGCCTCTATC
CATACCAAGGAGGCCAGCCTGGCCCTGAGCTGCTGGATACAGCTGGACCTGAATTCCTGA
TGCCCATGTGATGTTGTTGCCCCAGATGGGCACTAAATGGCCTCACTCCTTCCTGAAAAA
AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
AAAAAAAAAAAAAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_004658 unedited
GAAACGTCAGAATTTGTATACGACTCACTATAGGGCGGCCGCGAATTCGCACGAGGCCCC
GGGCACCTACACCTTCTCCTCTTTCGGAAATCTCCCATCCAGCTACCCGGGTCTCGGACA
GGCGGCACTGGGACCACGAGGCAGGGAGCCAGGCTTGAAGCAGGTGACATGTAGACGTCC
CCTGGTCCAGCCTCGGAACCTGAGCGCCCTTCTGCCTGGAAAGTTTGTGGCTAGGCGCCA
TGGCCAAGAGCAGCTCCCTGAATGTTCGCGTGGTGGAGGGCCGCGCGCTGCCTGCCAAGG
ACGTGTCTGGGAGCAGCGACCCCTACTGCCTAGTGAAAGTGGACGACGAGGTGGTGGCCA
GGACAGCTACTGTCTGGAGGAGCCTGGGCCCCTTCTGGGGGGAGGAGTACACGGTGCACC
TGCCTCTGGATTTCCACCAGCTGGCCTTCTACGTGCTGGATGAGGACACTGTCGGGCACG
ACGACATCATCGGCAAGATCTCGCTGAGCAGGGAGGCGATTACAGCCGACCCCCGAGGGA
TTGACAGCTGGATTAACTTGAGCCGAGTGGACCCAGATGCAGAAGTGCAGGGTGAGATCT
GCCTGTCAGTGCAGATGCTGGAGGATGGGCAGGGCCGCTGCCTTCGCTGCCATGTGCTTC
AGGCCAGGGACCTGGCTCCCAGAGACATCTCTGGCACATCTGACCCATTTGCACGTGTGT
TTTGGGGCAGCCAGAGCTTGGAGACCTCAACCATCAAGAAGACTCGCTTCCCGCACTGGG
ATGAAGTGCTGGAGCTGCNGGAGATGCCCAGTGCCCCGTCCCCCTGCGGGTGGAGCTCTG
GGACTGGGACATGGTGGGCAAGAATGACTTCTTGGGCATGGTGGAGTTCTCTCCAAACCC
TA
Restriction Sites Please inquire     
ACCN NM_004658
ORF Size 2415 bp
Insert Size 3028
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).
Reference Data
RefSeq NM_004658.1, NP_004649.1
RefSeq Size 3148
RefSeq ORF 2415
Locus ID 8437
Gene Summary The protein encoded by this gene is member of the GAP1 family of GTPase-activating proteins. These proteins stimulate the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. This particular family member contains domains which are characteristic of the GAP1 subfamily of RasGAP proteins but, in contrast to the other GAP1 family members, this protein is strongly and selectively expressed in endocrine tissues. Alternatively spliced transcript variants that encode different isoforms have been described [provided by RefSeq, Jul 2010]
Transcript Variant: This variant (2) differs in the 5' UTR and uses two alternate, in-frame splice sites in the coding region compared to variant 1. The resulting protein (isoform 2) is shorter but has the same N- and C-termini compared to 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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