×
For best experience we recommend to activate Javascript in your browser.
SGCD antibody
The Rabbit Polyclonal anti-SGCD antibody has been validated for IF. It is suitable to detect SGCD in samples from Human, Mouse and Rat.
Quick Overview for SGCD antibody (ABIN7256868)
Target
See all SGCD Antibodies
SGCD
(Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))
Reactivity
All reactivities for SGCD antibodies
Human, Mouse, Rat
Host
All hosts for SGCD antibodies
Rabbit
Clonality
All clonalities for SGCD antibodies
Polyclonal
Conjugate
All conjugates for SGCD antibodies
This SGCD antibody is un-conjugated
Application
All applications for SGCD antibodies
Immunofluorescence (IF)
Product Details anti-SGCD Antibody
(hide)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human SGCD (NP_000328.2).
Isotype
IgG
Alternatives
(show)
anti-Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD) (AA 37-86) antibody
SGCD
Reactivity: Human, Mouse, Rat, Cow, Rabbit, Guinea Pig, Bat, Pig, Hamster, Monkey
WB
Host: Rabbit
Polyclonal
unconjugated
Application Details
(hide)
Application Notes
IF 1:50-1:200
Restrictions
For Research Use only
Handling
(hide)
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 SGCD
(hide)
Target
SGCD
(Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))
Alternative Name
SGCD
Background
The protein encoded by this gene is one of the four known components of the sarcoglycan complex, which is a subcomplex of the dystrophin-glycoprotein complex (DGC). DGC forms a link between the F-actin cytoskeleton and the extracellular matrix. This protein is expressed most abundantly in skeletal and cardiac muscle. Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene.
Gene ID
6444
UniProt
Q92629
Pathways
Maintenance of Protein Location
Recently viewed
(hide)
Chat with us , powered by LiveChat