AdipoGen Life Sciences

anti-Fis1, pAb

As low as CHF 140.00
In stock
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AG-25B-0007V-TRIAL25 µgCHF 140.00
AG-25B-0007V-C100100 µgCHF 370.00

Specifications / Handling

More Information
Product Details
Synonyms Mitochondrial Fission 1 Protein; Tetratricopeptide Repeat Protein 11; TTC 11
Product Type Polyclonal Antibody
Properties
Source/Host Rabbit
Immunogen/Antigen Recombinant human Fis1.
Application

Immunocytochemistry: (methanol fixation; 1:200)
Immunoprecipitation: (1:200)
Western Blot: (1:500)

Crossreactivity Human
Mouse
Rat
Specificity

Recognizes human, mouse and rat Fis1.

Purity Detail Protein A-affinity purified.
Concentration 1mg/ml
Formulation Liquid. In PBS containing 10% glycerol and 0.02% sodium azide.
Isotype Negative Control

Rabbit IgG

Other Product Data

This purified antiserum is replacing the product AG-25B-0007 Fis-1 pAb (neat antiserum) with same specifications.

Declaration Manufactured by AdipoGen. Formerly sold as ALX-210-907 by ALEXIS Biochemicals.
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice After opening, prepare aliquots and store at -20°C.
Avoid freeze/thaw cycles.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
Documents
MSDS Download PDF Download PDF
Product Specification Sheet
Datasheet Download PDF Download PDF

Scientific Background Information

Product Description

Fis1 promotes the fragmentation of the mitochondrial network and its perinuclear clustering. It can induce cytochrome c release from mitochondria to the cytosol, ultimately leading to apoptosis. It also mediates peroxisomal fission.

Product-specific References
  1. hFis1, a novel component of the mammalian mitochondrial fission machinery: D.I. James, et al.; J. Biol. Chem. 278, 36373 (2003)
  2. A role for Fis1 in both mitochondrial and peroxisomal fission in mammalian cells: A. Koch, et al.; Mol. Biol. Cell 16, 5077 (2005)
  3. The Novel Tail-anchored Membrane Protein Mff Controls Mitochondrial and Peroxisomal Fission in Mammalian Cells.: S. Gandre-Babbe & AM. van der Bliek; Mol. Biol. Cell 6, 2402 (2008)
  4. Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28: A. Mignarri, et al.; J. Neurol. Sci. 362, 287 (2016)
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