OriGene Logo

Customer Login

Checkout as a new customer

Creating an account has many benefits:

  • See order and shipping status
  • Track order history
  • Check out faster
Create an Account

NBPF15 (NM_173638) Human Tagged ORF Clone Lentiviral Particle

  • LentiORF®
  • Product Brand Image
Be the first to review this product
SKU
RC212377L2V
Lenti ORF particles, NBPF15 (mGFP-tagged) - Human neuroblastoma breakpoint family, member 15 (NBPF15), transcript variant 2, 200ul, >10^7 TU/mL
  $1,470.00
3 Weeks*
Bulk Requests & Clone Modifications

Frequently Bought Together (2)

TR30038 One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
96 reactions
$700.00
PS100071V Lenti ORF control particles of pLenti-C-mGFP, 10^7 TU/mL, 0.5 mL
500 ul
$380.00

Other products for "NBPF15 or NM_173638"

Specifications
Specifications
Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Target Symbol NBPF15
Synonyms AB14; AG3; NBPF16
Vector pLenti-C-mGFP
Mammalian Cell Selection None
Sequence Data
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC212377).
ACCN NM_173638
ORF Size 2010 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_173638.2, NP_775909.1
RefSeq Size 4272 bp
RefSeq ORF 2013 bp
Locus ID 284565
UniProt ID Q8N660
Cytogenetics 1q21.1
MW 77.5 kDa
Summary This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. provided by RefSeq, May 2013
Reviews
Write Review
 
 
 
 
 

Be the first to review this product

Please note:
Only reviews with images are eligible for a $20/20€ Amazon gift card.
Reviews without images are eligible for a $10/10€ Amazon gift card.
For more details about the terms and conditions, please visit the promotion page.

Review image
Documents
Resources

file-alt Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Related Products