Comparison

DDB1 Polyclonal Antibody

Item no. E-AB-60795-200
Manufacturer Elabscience
Amount 200 uL
Quantity options 120 uL 200 uL 60 uL
Category
Type Antibody Polyclonal
Applications IF, IHC
Specific against Human (Homo sapiens), Mouse (Murine, Mus musculus), Rat (Rattus norvegicus)
Host Rabbit
Isotype IgG
Conjugate/Tag Unconjugated
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias DDB1, DDBA, UV-DDB1, XAP1, XPCE, XPE, XPE-BF
Similar products DDB1, Ddb1, XAP1, XPE, XPE-BF, DDB p127 subunit, DNA damage-binding protein 1, DDB 1, DDBa, DNA damage binding protein 1, UV damaged DNA binding factor, UV damaged DNA binding protein 1, UV DDB 1, X associated protein 1, XAP 1, Xeroderma pigmentosum group E complementing protein, XPE binding factor, HBV X-associated protein 1, XAP-1, XPE-binding factor, UV-damaged DNA-binding factor, DNA damage-binding protein a, UV-DDB 1, UV DDB1, XPE BF, Damage specific DNA binding protein 1, Damage-specific DNA-binding protein 1, UV-damaged DNA-binding protein 1, Xeroderma pigmentosum group E-complementing protein, XPCe
Shipping Condition Cool pack
Hazard information Comply with cargo safety certificate
Available
Manufacturer - Category
Primary Antibodies
Manufacturer - Targets
DDB1
Shipping Temperature
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Calculated Molecular Weight
50kDa/126kDa
Observed Molecular Weight
127kDa
Manufacturer - Research Areas
Cancer, Epigenetics and Nuclear Signaling
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.
Concentration
1mg/mL
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Purification Method
Affinity purification
Recommended Dilution
IHC 1:50-1:100; IF 1:50-1:100
Abbreviation
DDB1
Clonality
Polyclonal
Immunogen
A synthetic peptide of human DDB1
Category ID III
Polyclonal Antibodies

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 200 uL
Available: In stock
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