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ERCC2 antibody
The Rabbit Polyclonal anti-ERCC2 antibody (ABIN7261588) specifically detects ERCC2 in IF.
The antibody is reactive with Human and Rat samples.
Catalog No. ABIN7261588
$696.00
Plus shipping costs $50.00
60 μL ABIN7010744
120 μL ABIN7261587
200 μL ABIN7261588
60 μL ABIN7010744
120 μL ABIN7261587
200 μL ABIN7261588
Delivery in 11 to 15 Business Days
Quick Overview for ERCC2 antibody (ABIN7261588)
Target
See all ERCC2 Antibodies
ERCC2
(Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
Reactivity
All reactivities for ERCC2 antibodies
Human, Rat
Host
All hosts for ERCC2 antibodies
Rabbit
Clonality
All clonalities for ERCC2 antibodies
Polyclonal
Conjugate
All conjugates for ERCC2 antibodies
This ERCC2 antibody is un-conjugated
Application
All applications for ERCC2 antibodies
Immunofluorescence (IF)
Product Details anti-ERCC2 Antibody
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Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human ERCC2 (NP_001124339.1).
Isotype
IgG
Alternatives
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Application Details
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Application Notes
IF 1:50-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for ERCC2
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Target
ERCC2
(Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
Alternative Name
ERCC2
Background
The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Gene ID
2068
UniProt
P18074
Pathways
DNA Damage Repair
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anti-ERCC2 antibody (ABIN7261588)
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