ARG56346

anti-delta Sarcoglycan antibody

anti-delta Sarcoglycan antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes delta Sarcoglycan
Tested Reactivity Hu, Ms, Rat
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name delta Sarcoglycan
Antigen Species Human
Immunogen Recombinant protein of Human delta Sarcoglycan
Conjugation Un-conjugated
Alternate Names DAGD; 35DAG; SG-delta; Delta-sarcoglycan; Delta-SG; CMD1L; 35 kDa dystrophin-associated glycoprotein; SGCDP; SGD

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:200
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Jurkat

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
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. 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: 24052 Mouse SGCD

GeneID: 6444 Human SGCD

Swiss-port # P82347 Mouse Delta-sarcoglycan

Swiss-port # Q92629 Human Delta-sarcoglycan

Gene Symbol SGCD
Gene Full Name sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
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. [provided by RefSeq, Jul 2008]
Function Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix. [UniProt]
Calculated MW 32 kDa
PTM Glycosylated.
Disulfide bonds are present.