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MYOZ2 antibody
MYOZ2
Reactivity: Human, Mouse, Rat
IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-MYOZ2 Antibody
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Target
See all MYOZ2 Antibodies
MYOZ2
(Myozenin 2 (MYOZ2))
Reactivity
All reactivities for MYOZ2 antibodies
Human, Mouse, Rat
Host
All hosts for MYOZ2 antibodies
Rabbit
Clonality
All clonalities for MYOZ2 antibodies
Polyclonal
Conjugate
All conjugates for MYOZ2 antibodies
This MYOZ2 antibody is un-conjugated
Application
All applications for MYOZ2 antibodies
Immunofluorescence (IF)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human MYOZ2 (NP_057683.1).
Isotype
IgG
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Discover our top product MYOZ2 Primary Antibody
Alternatives
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Application Details
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Application Notes
IF 1:50-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for MYOZ2
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Target
MYOZ2
(Myozenin 2 (MYOZ2))
Alternative Name
MYOZ2 (MYOZ2 Products )
Synonyms
LOC733663 antibody, myoz2 antibody, MGC52797 antibody, cs-1 antibody, myozenin-2 antibody, MYOZ2 antibody, Myozenin-2 antibody, DKFZp468M0519 antibody, 1110012I24Rik antibody, Fatz-2 antibody, Myozl2 antibody, C4orf5 antibody, CMH16 antibody, CS-1 antibody, myozenin 2 antibody, myozenin 2 S homeolog antibody, myozenin 2 L homeolog antibody, MYOZ2 antibody, myoz2.S antibody, myoz2.L antibody, myoz2 antibody, Myoz2 antibody
Background
The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.
Gene ID
51778
UniProt
Q9NPC6
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