ID2 (NM_002166) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC205324L2V
- LentiORF®
-
Lenti ORF particles, ID2 (mGFP-tagged) - Human inhibitor of DNA binding 2, dominant negative helix-loop-helix protein (ID2), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | ID2 |
Synonyms | bHLHb26; GIG8; ID2A; ID2H |
Vector | pLenti-C-mGFP |
ACCN | NM_002166 |
ORF Size | 402 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC205324).
|
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_002166.4, NP_002157.2 |
RefSeq Size | 1402 bp |
RefSeq ORF | 405 bp |
Locus ID | 3398 |
Cytogenetics | 2p25.1 |
Domains | HLH |
Protein Families | ES Cell Differentiation/IPS, Stem cell relevant signaling - TGFb/BMP signaling pathway, Transcription Factors |
Protein Pathways | TGF-beta signaling pathway |
MW | 14.9 kDa |
Gene Summary | 'The protein encoded by this gene belongs to the inhibitor of DNA binding family, members of which are transcriptional regulators that contain a helix-loop-helix (HLH) domain but not a basic domain. Members of the inhibitor of DNA binding family inhibit the functions of basic helix-loop-helix transcription factors in a dominant-negative manner by suppressing their heterodimerization partners through the HLH domains. This protein may play a role in negatively regulating cell differentiation. A pseudogene of this gene is located on chromosome 3. [provided by RefSeq, Aug 2011]' |
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