Products for Research Use Only

Cofilin 2 Rabbit Polyclonal Antibody

CAT: 0013-GTR18307216Size: 100 µLDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR18307216Size:100 µL
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Rabbit polyclonal antibody to Cofilin 2
Product Name Alternative
Cofilin 2 , NEM7
UniProt
Q9Y281
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant protein encompassing a sequence within the center region of human Cofilin 2. The exact sequence is proprietary.
Target
Cofilin 2
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Musculoskeletal & Connective Tissue Research
Purification
Purified by antigen-affinity chromatography.
Concentration
0.28 mg/ml
Dilution
WB: 1:500-1:3000 , IF: 1:100-1:1000
Purity
Purified by antigen-affinity chromatography.
Form
Liquid: 1XPBS, 1% rAlbumin, 20% Glycerol (pH7) . 0.025% ProClin 300 was added as a preservative.
Molecular Weight
19
Storage Conditions
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°lC or below. Avoid multiple freeze-thaw cycles.
Notes
For research use only.
Applications Notes
Positive control: Mouse brain , rat heart , H1299 , HCT116
Tested Applications
ICC, WB
Host or Source
Rabbit
Preservative
PBS, 1% rAlbumin, 20% Glycerol, 0.025% ProClin 300.
Isotype
IgG

UniProtKB · Q9Y281

Cofilin-2

COF2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9Y281
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CFL2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
G3V5P4
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Molecular function

Actin-binding

Coding sequence diversity

Alternative splicing

Cellular component

CytoplasmCytoskeletonNucleus

Disease

Disease variantNemaline myopathy