Mouse Anti-TDP1 Recombinant Antibody (2A10-G2) (CBMAB-A8989-LY)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Biological Process double-strand break repairIDA:UniProtKB1 Publication
Biological Process single strand break repairIDA:UniProtKB1 Publication
Cytoplasm
A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAN1 is an autosomal recessive cerebellar ataxia (ARCA) associated with peripheral axonal motor and sensory neuropathy, distal muscular atrophy, pes cavus and steppage gait as seen in Charcot-Marie-Tooth neuropathy. All affected individuals have normal intelligence.
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
Antibody Pairs
TDP1 Matched Antibody Pair (1193) (CAT#: APMAB-1193LY)
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Mouse Anti-TDP1 Recombinant Antibody (CBYJT-2449) (CAT#: CBMAB-T1595-YJ)
TDP1 Matched Antibody Pair (1194) (CAT#: APMAB-1194LY)
TDP1 Matched Antibody Pair (1193) (CAT#: APMAB-1193LY)
Rabbit Anti-TDP1 Recombinant Antibody (CBYJT-2453) (CAT#: CBMAB-T1600-YJ)
Mouse Anti-TDP1 Recombinant Antibody (CBYJT-2452) (CAT#: CBMAB-T1599-YJ)
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Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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