Ataxin 2 ELISA Kits

ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human Ataxin 2 can be quantified in various samples, including cell lysate, plasma, serum, tissue homogenate.

Invitrogen ELISA kits exist in two formats: Uncoated and... ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human Ataxin 2 can be quantified in various samples, including cell lysate, plasma, serum, tissue homogenate.

Invitrogen ELISA kits exist in two formats: Uncoated and Coated.... ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human Ataxin 2 can be quantified in various samples, including cell lysate, plasma, serum, tissue homogenate.

Invitrogen ELISA kits exist in two formats: Uncoated and Coated. Uncoated ELISA kits include all the necessary reagents to coat your own plates and run your assay with maximum flexibility. Coated ELISA kits... ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human Ataxin 2 can be quantified in various samples, including cell lysate, plasma, serum, tissue homogenate.

Invitrogen ELISA kits exist in two formats: Uncoated and Coated. Uncoated ELISA kits include all the necessary reagents to coat your own plates and run your assay with maximum flexibility. Coated ELISA kits are ready-to-use and quality tested for sensitivity, specificity, precision and lot-to-lot consistency.

Target Information

The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. Defects in this gene are the cause of spinocerebellar ataxia type 2 (SCA2). SCA2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. SCA2 is caused by expansion of a CAG repeat in the coding region of this gene. Longer expansions result in earlier onset of the disease. Alternatively spliced transcript variants encoding different isoforms have been identified but their full length sequence has not been determined.

Synonyms

9630045M23Rik; ASL13; ataxin 2; ataxin-2; ATX2; Atxn2; AW544490; FLJ46772; Sca2; spinocerebellar ataxia 2 (olivopontocerebellar ataxia 2, autosomal dominant, ataxin 2); spinocerebellar ataxia 2 homolog; spinocerebellar ataxia type 2 protein; Spinocerebellar ataxia type 2 protein homolog; TNRC13; Trinucleotide repeat-containing gene 13 protein

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Invitrogen

Human ATXN2 ELISA Kit

Invitrogen

Human ATXN2 ELISA Kit

Sensitivity 0.47 ng/mL

Assay Range 0.78-50 ng/mL

Sample Volume

Cell Lysate

100 µL

Plasma

100 µL

Tissue Homogenate

100 µL

Time To Result

3 hr 30 min

(1 hr 20 min hands-on)

Price

Cat # EEL170

96 Tests

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Ataxin 2 ELISA Kits

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