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Anti-SETX / Senataxin Antibody (Internal) LS-C145161

Ordering

Wt. Vol. Conc. Price
- 100 µl - $365
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular SETX / Senataxin Antibodies

Anti-SETX / Senataxin Antibody (aa2579-2677, AP) LS-C245730
Mouse Monoclonal (IgG1) to Human SETX / Senataxin
Human
ICC, Western blot, ELISA
AP Conjugated
Anti-SETX / Senataxin Antibody (aa2579-2677, Biotin) LS-C245731
Mouse Monoclonal (IgG1) to Human SETX / Senataxin
Human
ICC, Western blot, ELISA
Biotin Conjugated
Anti-SETX / Senataxin Antibody (aa2579-2677, PE) LS-C245734
Mouse Monoclonal (IgG1) to Human SETX / Senataxin
Human
ICC, Western blot, ELISA
PE Conjugated

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal to Human SETX / Senataxin
Human
ICC, Western blot, ELISA
Unconjugated

Details

Human SETX / Senataxin
Rabbit
Human (tested or 100% immunogen sequence identity)
Polyclonal
Unconjugated
Antiserum
Unmodified

Applications

  • ICC
  • Western blot
  • ELISA

Specificity and Use

SETX / Senataxin antibody was raised against synthetic peptides derived from internal domain of the human SETX protein
Internal
Human 303 kD protein

Packaging

Lyophilized antiserum
100 µl Distilled water
Store lyophilized at -20°C for 2 years. Stable at 4°C for at least one month or for six months in aliquots at -20°C. Avoid freeze/thaw cycles.
For research use only.

About SETX / Senataxin

Q7Z333 NM_015046 NP_055861.3

SETX Antibody, AOA2 Antibody, KIAA0625 Antibody, ALS4 Antibody, SCAR1 Antibody, BA479K20.2 Antibody, Probable helicase senataxin Antibody, SEN1 homolog Antibody, Senataxin Antibody

SETX / Senataxin is a protein named for its homology to the Sen1p protein of fungi which has RNA helicase activity encoded by a domain at the C-terminal end of the protein. The protein encoded by this gene contains a DNA/RNA helicase domain at its C-terminal end which suggests that it may be involved in both DNA and RNA processing. Mutations in this gene have been associated with ataxia-ocular apraxia-2 (AOA2) and an autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS4).

Requested From: United States
Date Requested: 12/3/2016

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