Lactate Dehydrogenase B (LDHB) (NM_002300) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC205074L2V

  • LentiORF®

Lenti ORF particles, LDHB (mGFP-tagged) - Human lactate dehydrogenase B (LDHB), transcript variant 1, 200ul, >10^7 TU/mL

Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 820.00

6 Weeks*

Size
    • 200 ul

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol LDHB
Synonyms HEL-S-281; LDH-B; LDH-H; LDHBD; TRG-5
Vector pLenti-C-mGFP
ACCN NM_002300
ORF Size 1002 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC205074).
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_002300.3, NP_002291.1
RefSeq Size 1336 bp
RefSeq ORF 1005 bp
Locus ID 3945
Cytogenetics 12p12.1
Domains ldh
Protein Families Druggable Genome
Protein Pathways Cysteine and methionine metabolism, Glycolysis / Gluconeogenesis, Metabolic pathways, Propanoate metabolism, Pyruvate metabolism
MW 36.5 kDa
Gene Summary 'This gene encodes the B subunit of lactate dehydrogenase enzyme, which catalyzes the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+ in a post-glycolysis process. Alternatively spliced transcript variants have been found for this gene. Recent studies have shown that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Mutations in this gene are associated with lactate dehydrogenase B deficiency. Pseudogenes have been identified on chromosomes X, 5 and 13. [provided by RefSeq, Feb 2016]'

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