SHISA5 (NM_001272083) Human Untagged Clone

CAT#: SC333206

SHISA5 (untagged) - Homo sapiens shisa family member 5 (SHISA5), transcript variant 7


  "NM_001272083" in other vectors (2)

Reconstitution Protocol

USD 310.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol SHISA5
Synonyms SCOTIN
Vector pCMV6 series
Sequence Data
>NCBI ORF sequence for NM_001272083, the custom clone sequence may differ by one or more nucleotides


ATGGGGTTCGGAGCGACCTTGGCCGTTGGCCTGACCATCTTTGTGCTGTCTGTCGTCACTATCATCATCT
GCTTCACCTGCTCCTGCTGCTGCCTTTACAAGACGTGCCGCCGACCACGTCCGGTTGTCACCACCACCAC
ATCCACCACTGTGGTGCATGCCCCTTATCCTCAGCCTCCAAGTGTGCCGCCCAGCTACCCTGGACCAAGC
TACCAGGGCTACCACACCATGCCGCCTCAGCCAGGGATGCCAGCAGCACCCTACCCAATGCAGTACCCAC
CACCTTACCCAGCCCAGCCCATGGGCCCACCGGCCTACCACGAGACCCTGGCTGGTGAGTGCCCCTGCCA
ACTCTAG


Restriction Sites SgfI-MluI     
ACCN NM_001272083
ORF Size 357 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_001272083.1, NP_001259012.1
RefSeq Size 2216
RefSeq ORF 357
Locus ID 51246
Protein Families Transmembrane
Protein Pathways p53 signaling pathway
Gene Summary This gene encodes a member of the shisa family. The encoded protein is localized to the endoplasmic reticulum, and together with p53 induces apoptosis in a caspase-dependent manner. Alternative splicing results in multiple transcript variants. Related pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Apr 2016]
Transcript Variant: This variant (7) contains an alternate 5' terminal exon, initiates translation at an alternate start codon, and differs at the 3' end compared to variant 1. The encoded isoform (e) has distinct N- and C- termini and is shorter than isoform a.

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