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Fanconi Anemia Complementation Group G (FANCG) ELISA Kits

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). Additionally we are shipping Fanconi Anemia Complementation Group G Antibodies (126) and Fanconi Anemia Complementation Group G Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
FANCG 2189 O15287
FANCG 60534 Q9EQR6
Anti-Rat FANCG FANCG 691105  
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Top Fanconi Anemia Complementation Group G ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human
96 Tests Log in to see 11 to 13 Days
$875.60
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Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details

More ELISA Kits for Fanconi Anemia Complementation Group G Interaction Partners

Xenopus laevis Fanconi Anemia Complementation Group G (FANCG) interaction partners

  1. Identification of the Xenopus laevis ortholog of human FANCG (xFANCG), its expression during development, and its molecular interactions with a partner protein, xFANCA

Human Fanconi Anemia Complementation Group G (FANCG) interaction partners

  1. Patients, homozygous for the FANCG founder mutation, present with severe cytopenia but progress to bone marrow failure at similar ages to other individuals affected with Fanconi anemia (show PALB2 ELISA Kits) of heterogeneous genotype.

  2. founder haplotype analysis of FANCG for the Korean Fanconi anemia (show PALB2 ELISA Kits) population

  3. A new role of FANCG in Homologous recombination repair of interstrand crosslinks through K63Ub-mediated interaction with the Rap80-BRCA1 complex.

  4. FANCA (show FANCA ELISA Kits) and FANCG are the major Fanconi anemia (show PALB2 ELISA Kits) genes in the Korean population.

  5. Areca nut extracts-induced miR (show MLXIP ELISA Kits)-23a was correlated with a reduced FANCG expression and DSB repair, which might contribute to ANE-associated human malignancies.

  6. sites of interaction of FANCG with ERCC1 (show ERCC1 ELISA Kits), which is different from the region of ERCC1 (show ERCC1 ELISA Kits) that binds to XPF (show ERCC4 ELISA Kits)

  7. Study of the molecular evolution of FA genes using database search methods such as PSI-BLAST suggested that FANCG may contain a known domain, and that this protein is a member of the family of tetratricopeptide repeat-containing proteins.

  8. There is remarkably lage sequence variation in FANCG gene mutations and polymorphisms across ethnic and racial backgrounds found in the International Fanconi Anemia (show PALB2 ELISA Kits) Registry they include IVS8-2A>G, IVS11+1G>c, 1794_1803del10, and IVS3+1G>C.

  9. FANCG was able to mediate interaction between FANCA (show FANCA ELISA Kits) and FANCF, as well as between monomers of FANCA (show FANCA ELISA Kits)

  10. FANCG is required for efficient homologous recombination-mediated repair of at least some types of DNA double-strand breaks

Mouse (Murine) Fanconi Anemia Complementation Group G (FANCG) interaction partners

  1. Hematopoietic stem cells of Fancg-/- mice Impaired functionality and homing.

  2. null mutations in Fanca (show FANCA ELISA Kits) or Fancg are fully epistatic

  3. the FA pathway (FancG) is not involved in regulating the outcome of SHM (show CNTNAP1 ELISA Kits) in mammals and it appears dispensable for class switch recombination

  4. Data show that Fancd2 (show FANCD2 ELISA Kits)(-/-) mice displayed a higher magnitude of chromosomal breakage and micronucleus formation than the wild-type or Fancg(-/-) mice.

  5. Double-mutant Fancc (show FANCC ELISA Kits)(-/-);Fancg(-/-) mice develop spontaneous hematologic sequelae including bone marrow failure, acute myeloid leukemia (show BCL11A ELISA Kits), myelodysplasia and complex random chromosomal abnormalities that the single-mutant mice do not.

  6. Mice deficient in Fancg were not anemic, but showed hypogonadism, impaired fertility, and hypersensitivity to mitomycin C

  7. FANCG is required for efficient homologous recombination-mediated repair of at least some types of DNA double-strand breaks

  8. Fancg deeficient mouse cells display normal telomere length, normal telomerase activity, and normal chromosome end-capping

  9. a deletion mutation in the FANCG gene (c.637_643delTACCGCC) was present in 82% of Fanconi anemia (show PALB2 ELISA Kits) patients in the black populations of Southern Africa

  10. Ataxia telangiectasia mutated (show ATM ELISA Kits) and Fanconi anemia (show PALB2 ELISA Kits) genes function in parallel and compensatory roles to maintain genomic integrity and cell viability.

Fanconi Anemia Complementation Group G (FANCG) Antigen Profile

Antigen 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 G.

Gene names and symbols associated with FANCG

  • Fanconi anemia, complementation group G (fancg) antibody
  • Fanconi anemia, complementation group G (FANCG) antibody
  • Fanconi anemia, complementation group G (Fancg) antibody
  • AU041407 antibody
  • FAG antibody
  • xFANCG antibody
  • Xrcc9 antibody

Protein level used designations for FANCG

Fanconi anemia complementation group G variant 2 , DNA repair protein XRCC9 , Fanconi anemia group G protein , X-ray repair complementing defective repair in Chinese hamster cells 9 , X-ray repair, complementing defective, in Chinese hamster, 9 , Fanconi anemia group G protein homolog

GENE ID SPECIES
100125673 Xenopus laevis
2189 Homo sapiens
60534 Mus musculus
611887 Canis lupus familiaris
100511060 Sus scrofa
615352 Bos taurus
691105 Rattus norvegicus
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