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- Home > Products > MaxPab® Ab > Human > Binding > Others > SGCD MaxPab mouse polyclonal antibody (B01)
SGCD MaxPab mouse polyclonal antibody (B01) 
- 目录号 # : H00006444-B01
- 访问频率 :
- 尺寸
- 价格
- 库存
- 可得性
- 购物车
- 50 uL
- USD $ 319
- order now, ship next day
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Email : sales@abnova.com
Phone : +886-2-87511888
Fax : +886-2-87511166- 产品会直接装运至客户处。
- Specification
- Product Description:
- Mouse polyclonal antibody raised against a full-length human SGCD protein.
- Immunogen:
- SGCD (NP_000328.2, 1 a.a. ~ 290 a.a) full-length human protein.
- Sequence:
- MMPQEQYTHHRSTMPGSVGPQVYKVGIYGWRKRCLYFFVLLLMILILVNLAMTIWILKVMNFTIDGMGNLRITEKGLKLEGDSEFLQPLYAKEIQSRPGNALYFKSARNVTVNILNDQTKVLTQLITGPKAVEAYGKKFEVKTVSGKLLFSADNNEVVVGAERLRVLGAEGTVFPKSIETPNVRADPFKELRLESPTRSLVMEAPKGVEINAEAGNMEATCRTELRLESKDGEIKLDAAKIRLPRLPHGSYTPTGTRQKVFEICVCANGRLFLSQAGAGSTCQINTSVCL
- Host:
- Mouse
- Reactivity:
- Human
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- Storage Buffer:
- No additive
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Note:
- For IHC and IF applications, antibody purification with Protein A will be needed prior to use.
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of SGCD expression in transfected 293T cell line (H00006444-T01) by SGCD MaxPab polyclonal antibody.
Lane 1: SGCD transfected lysate(31.9 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 6444
- GeneBank Accession#:
- NM_000337.4
- Protein Accession#:
- NP_000328.2
- Gene Name:
- SGCD
- Gene Alias:
- 35DAG,CMD1L,DAGD,MGC22567,SG-delta,SGCDP,SGD
- Gene Description:
- sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
- Gene Ontology:
- Hyperlink
- Gene 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)
