GTX64576
FANCL antibody
Cannot supply to this region.
- SKU:
- GTX64576
- Additional Names:
- FA complementation group L , FAAP43 , PHF9 , POG
- Application:
- WB, IHC-P
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Buffer:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-255 of human FANCL (NP_060532.2).
- Uniprot:
- Q9NW38
- Synonyms:
- E3 ubiquitin-protein ligase FANCL;FAAP43;Fanconi anemia complementation group L;fanconi anemia group L protein;fanconi anemia-associated polypeptide of 43 kDa;PHD finger protein 9;PHF9;POG;RING-type E3 ubiquitin transferase FANCL
- Extra Details:
- This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018]
- Shipping Conditions:
- Blue Ice