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Human FANCA activation kit by CRISPRa

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SKU
GA101517
FANCA CRISPRa kit - CRISPR gene activation of human FA complementation group A
  $1,657.00
4 Weeks*

Frequently Bought Together (2)

TA308599 Rabbit polyclonal antibody to FACA (Fanconi anemia, complementation group A)
100 ul
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RC223218 FANCA (Myc-DDK-tagged)-Human Fanconi anemia, complementation group A (FANCA), transcript variant 2
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Other products for "FANCA"

Specifications
Specifications
Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Target Symbol FANCA
Locus ID 2175
Components

GA101517G1, FANCA gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA101517G2, FANCA gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA101517G3, FANCA gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077
OTI Disclaimer These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPRa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.
Shipping Ambient
Reference Data
RefSeq NM_000135, NM_001018112, NM_001286167, NM_001351830
UniProt ID O15360
Synonyms FA; FA-H; FA1; FAA; FACA; FAH; FANCH
Summary The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. provided by RefSeq, Jul 2008
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Other Versions
SKU Description Size Price
KN421634 FANCA - KN2.0, Human gene knockout kit via CRISPR, non-homology mediated. 1 kit
$1,657.00

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*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.

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