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Anti-alpha Sarcoglycan Rabbit mAb [48T48D33]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R010430
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-alpha Sarcoglycan Rabbit mAb [48T48D33]
Anti-alpha Sarcoglycan Rabbit mAb [48T48D33]
Anti-alpha Sarcoglycan Rabbit mAb [48T48D33]
Product NameAnti-alpha Sarcoglycan 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
ReactivityRat, Human, Mouse
HostRabbit
ClonalityMonoclonal
Clone No.48T48D33
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human alpha Sarcoglycan
FormatAffinity purified monoclonal antibody supplied in PBS with 0.01% sodium azide and 50% glycerol, pH 7.3.
Synonyms50 DAG, 50 kDa dystrophin associated glycoprotein, 50 kDa dystrophin-associated glycoprotein, 50DAG, 50kD DAG, 59kDa, A2, adhalin, ADL, Alpha SG, Alpha-sarcoglycan, Alpha-SG, Asg, DAG2, DMDA2, Dystroglycan 2, Dystroglycan-2, LGMD2D, sarcoglycan, alpha (dystrophin-associated glycoprotein), SCARMD1, Sgca, SGCA_HUMAN.
Molecular weightCalculated MW: 43 kDa; Observed MW: 50 kDa
Uniprot ID Q16586
Gene ID 6442
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-alpha Sarcoglycan Rabbit mAb [48T48D33] is for research use only and not for use in diagnostic or therapeutic procedures.
Background This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
Cellular Location Cell membrane > sarcolemma. Cytoplasm > cytoskeleton.
Tissue Location Most strongly expressed in skeletal muscle. Also expressed in cardiac muscle and, at much lower levels, in lung. In the fetus, most abundant in cardiac muscle and, at lower levels, in lung. Also detected in liver and kidney. Not expressed in brain.

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