Background:

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.

Classification:

Primary antibody

Alternative names:

FANCB

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human FANCB

Concentration:

1 mg/ml

Molecular weight:

94490

Applications:

WB

Storage:

-20°C for 1 year

More info:

Email: info@sobekbio.com

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