This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FANCBBA-20-REGO | 20 (40 μL) | 200 μL |
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| FANCBBA-20-REGR | 20 (40 μL) | 200 μL |
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| FANCBBA-20-ORGR | 20 (40 μL) | 200 μL |
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| FANCBBA-20-GOGR | 20 (40 μL) | 200 μL |
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| FANCBBA-20-GRRE | 20 (40 μL) | 200 μL |
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| FANCBBA-20-GROR | 20 (40 μL) | 200 μL |
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| FANCBBA-20-GRGO | 20 (40 μL) | 200 μL |
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| FANCBBA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
Gene Symbol : FANCB
Gene Name : Fanconi anemia complementation group B
Chromosome : CHR X: 148,732,54-146,908,62
Locus : Xp22.2
Alt. Genes : ENAM
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