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Guinea Pig Alpha-sarcoglycan (SGCA) ELISA Kit | SGCA elisa kit

Guinea pig Alpha-sarcoglycan (SGCA) ELISA Kit

Gene Names
SGCA; A2; ADL; DAG2; DMDA2; 50-DAG; LGMD2D; SCARMD1; adhalin
Reactivity
Guinea Pig
Synonyms
Alpha-sarcoglycan (SGCA); Guinea pig Alpha-sarcoglycan (SGCA) ELISA Kit; SGCA elisa kit
Ordering
For Research Use Only!
Reactivity
Guinea Pig
Samples
Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Preparation and Storage
Store all reagents at 2-8 degree C.
Product Categories/Family for SGCA elisa kit

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
Molecular Weight
29,354 Da
NCBI Official Full Name
alpha-sarcoglycan isoform 2
NCBI Official Synonym Full Names
sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
NCBI Official Symbol
SGCA
NCBI Official Synonym Symbols
A2; ADL; DAG2; DMDA2; 50-DAG; LGMD2D; SCARMD1; adhalin
NCBI Protein Information
alpha-sarcoglycan; 50DAG; 50kD DAG; alpha-SG; dystroglycan-2; 50 kDa dystrophin-associated glycoprotein
UniProt Protein Name
Alpha-sarcoglycan
Protein Family
UniProt Gene Name
SGCA
UniProt Synonym Gene Names
ADL; DAG2; Alpha-SG; 50DAG
UniProt Entry Name
SGCA_HUMAN

NCBI Description

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]

Uniprot Description

SGCA: 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. Defects in SGCA are the cause of limb-girdle muscular dystrophy type 2D (LGMD2D); also known as Duchenne- like muscular dystrophy autosomal recessive type 2 or severe childhood autosomal recessive muscular dystrophy (SCARMD). LGMD2D is an autosomal recessive degenerative myopathy characterized by progressive muscle wasting from early childhood with loss of independent ambulation by teenage years. Muscle biopsy shows necrosis, decreased immunostaining for alpha sarcoglycan, and adhalin deficiency. The phenotype is less severe than LGMD2C. Belongs to the sarcoglycan alpha/epsilon family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Motility/polarity/chemotaxis; Membrane protein, integral

Chromosomal Location of Human Ortholog: 17q21

Cellular Component: dystrophin-associated glycoprotein complex; cytoskeleton; cytoplasm; integral to membrane; sarcoglycan complex; intercellular junction; sarcolemma; lipid raft

Molecular Function: calcium ion binding

Biological Process: muscle development; muscle contraction

Disease: Muscular Dystrophy, Limb-girdle, Type 2d

Research Articles on SGCA

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Product Notes

The Guinea Pig SGCA sgca (Catalog #AAA7241834) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA7241834 ELISA Kit recognizes Guinea Pig SGCA. It is sometimes possible for the material contained within the vial of "Alpha-sarcoglycan (SGCA), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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