KLF4 (NM_004235) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC206691L2V
- LentiORF®
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Lenti ORF particles, KLF4 (mGFP-tagged) - Human Kruppel-like factor 4 (gut) (KLF4), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | KLF4 |
Synonyms | EZF; GKLF |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_004235 |
ORF Size | 1410 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC206691).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_004235.3, NP_004226.2 |
RefSeq Size | 2639 bp |
RefSeq ORF | 1440 bp |
Locus ID | 9314 |
UniProt ID | O43474 |
Cytogenetics | 9q31.2 |
Domains | zf-C2H2 |
Protein Families | Adult stem cells, Embryonic stem cells, ES Cell Differentiation/IPS, Induced pluripotent stem cells, Transcription Factors |
MW | 49.9 kDa |
Gene Summary | This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is required for normal development of the barrier function of skin. The encoded protein is thought to control the G1-to-S transition of the cell cycle following DNA damage by mediating the tumor suppressor gene p53. Mice lacking this gene have a normal appearance but lose weight rapidly, and die shortly after birth due to fluid evaporation resulting from compromised epidermal barrier function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015] |
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