DDB2 polyclonal, anti-human, mouse
€295.00
In stock
SKU
K006726P
Catalog Number: K006726P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: IHC
Request Manual
Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: IHC
Request Manual
Questions? Contact us!
Background:
This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene.
Synonyms: XPE, DDBB, UV-DDB2
Cellular Location: Nucleus
Immunogen:
Recombinant protein of human DDB2
Gene Symbol: DDB2
Gene ID: 1643
Swiss prot: Q92466
Calculated MW: 48kDa
Recommended dilution:
IHC 1:30-150
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene.
Synonyms: XPE, DDBB, UV-DDB2
Cellular Location: Nucleus
Immunogen:
Recombinant protein of human DDB2
Gene Symbol: DDB2
Gene ID: 1643
Swiss prot: Q92466
Calculated MW: 48kDa
Recommended dilution:
IHC 1:30-150
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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