ARG63822

anti-Cofilin 2 antibody

anti-Cofilin 2 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Rat

Signaling Transduction antibody

Overview

Product Description Goat Polyclonal antibody recognizes Cofilin 2
Tested Reactivity Hu, Rat
Predict Reactivity Ms, Dog, Pig
Tested Application IHC-P, WB
Specificity This antibody is expected to recognise both reported isoforms (NP_068733 and NP_619579)
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name Cofilin 2
Antigen Species Human
Immunogen C-DIKDRSTLGEK
Conjugation Un-conjugated
Alternate Names Cofilin, muscle isoform; NEM7; Cofilin-2

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P3 - 5 µg/ml
WB0.01 - 0.03 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by antigen affinity chromatography.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 1073 Human CFL2

Swiss-port # Q9Y281 Human Cofilin-2

Background This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH-dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]
Research Area Signaling Transduction antibody
Calculated MW 19 kDa
PTM The phosphorylation of Ser-24 may prevent recognition of the nuclear localization signal.