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ProductsBack/LAMP1 antibody

WB analysis of 20 microg of HeLa cell lysate using GTX19294 LAMP1 antibody. Dilution : 1:500

WB analysis of 20 microg of HeLa cell lysate using GTX19294 LAMP1 antibody. Dilution : 1:500

WB analysis of 20 microg of HeLa cell lysate using GTX19294 LAMP1 antibody. Dilution : 1:500

LAMP1 antibody

GTX19294

ApplicationsWestern Blot

Product group Antibodies

TargetLAMP1

Overview

Supplier
GeneTex
Product Name
LAMP1 antibody
Delivery Days Customer
9
Application Supplier Note
WB: 1:250 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
Applications
Western Blot
Certification
Research Use Only
Clonality
Polyclonal
Concentration
1 mg/ml
Conjugate
Unconjugated
Gene ID3916
Target name
LAMP1
Target description
lysosomal associated membrane protein 1
Target synonyms
CD107a, LAMPA, LGP120, lysosome-associated membrane glycoprotein 1, CD107 antigen-like family member A, lysosome-associated membrane protein 1
Host
Rabbit
Isotype
IgG
Protein IDP11279
Protein Name
Lysosome-associated membrane glycoprotein 1
Scientific Description
The protein encoded by this gene is a member of a family of membrane glycoproteins. This glycoprotein provides selectins with carbohydrate ligands. It may also play a role in tumor cell metastasis. [provided by RefSeq, Jul 2008]
Storage Instruction
-20°C or -80°C,2°C to 8°C
UNSPSC
12352203

References

Carballo-Carbajal I, Laguna A, Romero-Giménez J, et al. Brain tyrosinase overexpression implicates age-dependent neuromelanin production in Parkinson's disease pathogenesis. Nat Commun. 2019,10(1):973. doi: 10.1038/s41467-019-08858-y
Read this paper
Bové J, Martínez-Vicente M, Dehay B, et al. BAX channel activity mediates lysosomal disruption linked to Parkinson disease. Autophagy. 2014,10(5):889-900. doi: 10.4161/auto.28286
Read this paper
Dehay B, Bové J, Rodríguez-Muela N, et al. Pathogenic lysosomal depletion in Parkinson's disease. J Neurosci. 2010,30(37):12535-44. doi: 10.1523/JNEUROSCI.1920-10.2010
Read this paper

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