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Anti-Delta-sarcoglycan/SGCD Rabbit mAb [62I51Q05]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R016031
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-Delta-sarcoglycan/SGCD Rabbit mAb [62I51Q05]
Anti-Delta-sarcoglycan/SGCD Rabbit mAb [62I51Q05]
Anti-Delta-sarcoglycan/SGCD Rabbit mAb [62I51Q05]
Product NameAnti-Delta-sarcoglycan/SGCD Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P/IF (Tissue-P), ELISA
DilutionWB 1:1,000~1:2,000; IHC-P 1:100~1:200; IF 1:100~1:200
ReactivityHuman
HostRabbit
ClonalityMonoclonal
Clone No.62I51Q05
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human delta Sarcoglycan
FormatAffinity purified monoclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Synonyms35 kDa dystrophin associated glycoprotein; 35 kDa dystrophin-associated glycoprotein; 35DAG; CMD1L; DAGD; delta-sarcoglycan; delta-SG; Dystrophin associated glycoprotein delta sarcoglycan; LGMD2F; MGC22567; Placental delta sarcoglycan; Sarcoglycan delta(35 kDa dystrophin associated glycoprotein); SG delta; SGCD; SGCD_HUMAN; SGCDP; SGD.
Molecular weightCalculated MW: 32 kDa; Observed MW: 32 kDa
Uniprot ID Q92629
Gene ID 6444
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-Delta-sarcoglycan/SGCD Rabbit mAb [62I51Q05] is for research use only and not for use in diagnostic or therapeutic procedures.
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]
Cellular Location Cell membrane Sarcolemma Single-pass type II membrane protein Cytoplasm Cytoskeleton
Tissue Location Most strongly expressed in skeletal and cardiac muscle. Also detected in smooth muscle. Weak expression in brain and lung.

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