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Anti-FADD Antibody (phospho-Ser194) LS-C6763

Note: This antibody replaces LS-C6752

Ordering

Wt. Vol. Conc. Price
- 100 µl - $485
Inquire for larger quantities

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

Most Popular FADD Antibodies

Anti-FADD Antibody (phospho-Ser191) LS-C96871
Rabbit Polyclonal to Mouse FADD
Mouse
Western blot
Unconjugated
Western blot Image
Anti-FADD Antibody LS-C400744
Rabbit Polyclonal (IgG) to Human FADD
Human, Mouse
IHC, Western blot, ELISA
Unconjugated
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal (IgG) to Human FADD
Human
ICC, Western blot, ELISA
Unconjugated

Details

Human FADD
Rabbit
Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Unconjugated
Protein A purified
Unmodified

Applications

  • ICC
  • Western blot (1:1000)
  • ELISA

Specificity and Use

FADD antibody was raised against synthetic phosphopeptide (KLH coupled) corresponding to residues surrounding Ser194 of human FADD.
pSer194
Detects endogenous levels of human FADD protein only when phosphorylated at Ser194.
Suitable for use in ELISA, Immunocytochemistry and Western Blot. Western Blot: 1:1000, incubate membrane with diluted antibody in 5% BSA, 1X TBS, 0.1% Tween-20 at 4?C with gentle shaking, overnight. Immunocytochemistry (ABC): 1:200.

Packaging

10 mM HEPES, pH 7.5, 150 mM sodium chloride, 0.1 mg/ml BSA, 50% glycerol. No preservative added.
Long term: -20°C; Short term: +4°C. Avoid repeat freeze-thaw cycles.
For research use only.

About FADD

Q13158 NM_003824 NP_003815.1

FADD Antibody, GIG3 Antibody, MORT1 Antibody, Protein FADD Antibody

FADD is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors.

Requested From: United States
Date Requested: 12/4/2016

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