CYBB (NM_000397) Human Tagged ORF Clone Lentiviral Particle
SKU
RC207544L2V
Lenti ORF particles, CYBB (mGFP-tagged) - Human cytochrome b-245, beta polypeptide (CYBB), 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | mGFP |
Target Symbol | CYBB |
Synonyms | AMCBX2; CGD; CGDX; GP91-1; GP91-PHOX; GP91PHOX; IMD34; NOX2; p91-PHOX |
Vector | pLenti-C-mGFP |
Mammalian Cell Selection | None |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC207544).
|
ACCN | NM_000397 |
ORF Size | 1710 bp |
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. |
Shipping | Dry Ice |
Reference Data | |
RefSeq | NM_000397.2 |
RefSeq Size | 4353 bp |
RefSeq ORF | 1713 bp |
Locus ID | 1536 |
UniProt ID | P04839 |
Cytogenetics | Xp21.1-p11.4 |
Domains | Ferric_reduct |
Protein Families | Druggable Genome, Ion Channels: Other, Transmembrane |
Protein Pathways | Leukocyte transendothelial migration |
MW | 65.3 kDa |
Summary | Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain. It has been proposed as a primary component of the microbicidal oxidase system of phagocytes. CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte NADPH oxidase; neutrophils are able to phagocytize bacteria but cannot kill them in the phagocytic vacuoles. The cause of the killing defect is an inability to increase the cell's respiration and consequent failure to deliver activated oxygen into the phagocytic vacuole. [provided by RefSeq, Jul 2008] |
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