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LMAN1 (NM_005570) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC207088L4V
- LentiORF®
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Lenti ORF particles, LMAN1 (mGFP-tagged) - Human lectin, mannose-binding, 1 (LMAN1), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP
AAV Particle: DDK
Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50
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USD 365.00
Specifications
| Product Data | |
| Type | Human Tagged ORF Clone Lentiviral Particle |
| Tag | mGFP |
| Symbol | LMAN1 |
| Synonyms | ERGIC-53; ERGIC53; F5F8D; FMFD1; gp58; MCFD1; MR60 |
| Mammalian Cell Selection | Puromycin |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_005570 |
| ORF Size | 1530 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC207088).
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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_005570.2 |
| RefSeq Size | 4848 bp |
| RefSeq ORF | 1533 bp |
| Locus ID | 3998 |
| UniProt ID | P49257 |
| Cytogenetics | 18q21.32 |
| Domains | Lectin_leg-like |
| Protein Families | Druggable Genome, Transmembrane |
| MW | 57.5 kDa |
| Gene Summary | The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH-sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015] |
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