GSG1 (NM_001206843) Human Untagged Clone
CAT#: SC329843
GSG1 (untagged) - Homo sapiens germ cell associated 1 (GSG1), transcript variant 6
"NM_001206843" in other vectors (2)
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | GSG1 |
Synonyms | MGC3146; MGC111023 |
Vector | pCMV6 series |
Sequence Data |
>NCBI ORF sequence for NM_001206843, the custom clone sequence may differ by one or more nucleotides
ATGGCCAAGATGGAGCTCTCGAAGGCCTTCTCTGGCCAGCGGACACTCCTATCTGCCATCCTCAGCATGC TATCACTCAGCTTCTCCACAACATCCCTGCTCAGCAACTACTGGTTTGTGGGCACACAGAAGGTGCCCAA GCCCCTGTGCGAGAAAGGTCTGGCAGCCAAGTGCTTTGACATGCCAGTGTCCCTGGATGGAGATACCAAC ACATCCACCCAGGAGGTGGTACAATACAACTGGGAGACTGGGGATGACCGGTTCTCCTTCCGGAGCTTCC GGAGTGGCATGTGGCTATCCTGTGAGGAAACTGTGGAAGAACCAGCACTGCTCCATCCCCAGTCCTGGAA ACAATTTAGAGCCCTTCGGTCCAGTGGTACAGCGGCAGCAAAAGGGGAGAGGTGCCGAAGTTTCATTGAA CTTACACCACCAGCCAAGAGAGGTCTCCTGGGGATGGTGGCCCACATGATGTATTCACAAGTCTTCCAAG CGACTGTCAACTTGGGTCCAGAAGACTGGAGACCACATGTTTGGAATTATGGCTGGGCCTTCTACATGGC CTGGCTCTCCTTCACCTGCTGCATGGCGTCGGCTGTCACCACCTTCAACACGTACACCAGGATGGTGCTG GAGTTCAAGTGCAAGCATAGTAAGAGCTTCAAGGAAAACCCGAACTGCCTACCACATCACCATCAGTGTT TCCCTCGGCGGCTGTCAAGTGCAGCCCCCACCGTGGGTCCTTTGACCAGCTACCACCAGTATCATAATCA GCCCATCCACTCTGTCTCTGAGGGAGTCGACTTCTACTCCGAGCTGCGGAACAAGGGATTTCAAAGAGGG GCCAGCCAGGAGCTGAAAGAAGCAGTTAGGTCATCTGTAGAGGAAGAGCAGTGTTAG |
Restriction Sites | SgfI-MluI |
ACCN | NM_001206843 |
ORF Size | 897 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). |
Reference Data | |
RefSeq | NM_001206843.1, NP_001193772.1 |
RefSeq Size | 2460 |
RefSeq ORF | 897 |
Locus ID | 83445 |
Protein Families | Transmembrane |
Gene Summary | May cause the redistribution of PAPOLB from the cytosol to the endoplasmic reticulum. [UniProtKB/Swiss-Prot Function] Transcript Variant: This variant (6) includes an alternate in-frame exon in the central coding region and uses an alternate splice site that causes a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (6) has a distinct C-terminus and is longer than isoform 1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. |
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