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DDB1 Recombinant Rabbit mAb

Product Specifications

Background

The protein encoded by this gene is the large subunit (p127) of the heterodimeric DNA damage-binding (DDB) complex while another protein (p48) forms the small subunit. This protein complex functions in nucleotide-excision repair and binds to DNA following UV damage. Defective activity of this complex causes the repair defect in patients with xeroderma pigmentosum complementation group E (XPE) - an autosomal recessive disorder characterized by photosensitivity and early onset of carcinomas. However, it remains for mutation analysis to demonstrate whether the defect in XPE patients is in this gene or the gene encoding the small subunit. In addition, Best vitelliform mascular dystrophy is mapped to the same region as this gene on 11q, but no sequence alternations of this gene are demonstrated in Best disease patients. The protein encoded by this gene also functions as an adaptor molecule for the cullin 4 (CUL4) ubiquitin E3 ligase complex by facilitating the binding of substrates to this complex and the ubiquitination of proteins. [provided by RefSeq, May 2012]

CAS Number

9000-83-3

Structure Composition

Store at -20°C. Supplied in 50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.

Product Name Alternative

XPE; DDBA; XAP1; XPCE; XPE-BF; UV-DDB1

Swiss Prot

Q16531

Reactivity

Human, Mouse, Rat

Immunogen

A synthetic peptide of human DDB1

Conjugation

Unconjugated

Applications

WB, IHC, ICC/IF, IP

Purity

Affinity Purification

Modification

Unmodification

Molecular Weight

127 kDa

Storage Conditions

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Notes

For research use only, not for use in diagnostic procedure.

Specificity

IgG

Applications Notes

Western blot detection of DDB1 in Hela, MCF-7, HepG2, U2OS, U251, HL-60 using DDB1 antibody (1:1000 diluted) .

Host or Source

Rabbit

Available Sizes

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