SGCD (Human) Recombinant protein
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Specification
Product Description
Human SGCD (Q92629, 57 a.a. - 289 a.a) partial recombinant protein with His-tag at N-terminal expressed in Escherichia Coli.
Sequence
MGSSHHHHHH SSGLVPRGSH RSHMKVMNFT IDGMGNLRIT EKGLKLEGDS EFLQPLYAKE IQSRPGNALY FKSARNVTVN ILNDQTKVLT QLITGPKAVE AYGKKFEVKT VSGKLLFSAD NNEVVVGAER LRVLGAEGTV FPKSIETPNV RADPFKELRL ESPTRSLVME APKGVEINAE AGNMEATCRT ELRLESKDGE IKLDAAKIRL PRLPHGSYTP TGTRQKVFEI CVCANGRLFL SQAGAGSTCQ INTSVCL.
Host
Escherichia coli
Theoretical MW (kDa)
28
Form
Liquid
Preparation Method
Escherichia coli��expression system
Purity
> 85% by SDS-PAGE.
Storage Buffer
In 20mM Tris-HCl buffer, pH 8.0, 0.4M Urea and 10% glycerol.
Storage Instruction
Store at 4°C for 2~4 week. For long term storage store at -20°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
Aliquot to avoid repeated freezing and thawing. -
Applications
SDS-PAGE
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Gene Info — SGCD
Entrez GeneID
6444Protein Accession#
Q92629Gene Name
SGCD
Gene Alias
35DAG, CMD1L, DAGD, MGC22567, SG-delta, SGCDP, SGD
Gene Description
sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
Gene Ontology
HyperlinkGene Summary
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
Other Designations
35kD dystrophin-associated glycoprotein|delta-sarcoglycan|dystrophin associated glycoprotein, delta sarcoglycan|placental delta sarcoglycan|sarcoglycan, delta (35kD dystrophin-associated glycoprotein)
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Interactome
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Pathway
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Disease
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