GLRA1 purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
- More Functions
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human GLRA1 protein.
Immunogen
GLRA1 (NP_000162.2, 1 a.a. ~ 449 a.a) full-length human protein.
Sequence
MYSFNTLRLYLWETIVFFSLAASKEAEAARSAPKPMSPSDFLDKLMGRTSGYDARIRPNFKGPPVNVSCNIFINSFGSIAETTMDYRVNIFLRQQWNDPRLAYNEYPDDSLDLDPSMLDSIWKPDLFFANEKGAHFHEITTDNKLLRISRNGNVLYSIRITLTLACPMDLKNFPMDVQTCIMQLESFGYTMNDLIFEWQEQGAVQVADGLTLPQFILKEEKDLRYCTKHYNTGKFTCIEARFHLERQMGYYLIQMYIPSLLIVILSWISFWINMDAAPARVGLGITTVLTMTTQSSGSRASLPKVSYVKAIDIWMAVCLLFVFSALLEYAAVNFVSRQHKELLRFRRKRRHHKEDEAGEGRFNFSAYGMGPACLQAKDGISVKGANNSNTTNPPPAPSKSPEEMRKLFIQRAKKIDKISRIGFPMAFLIFNMFYWIIYKIVRREDVHNQ
Host
Rabbit
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of GLRA1 expression in transfected 293T cell line (H00002741-T02) by GLRA1 MaxPab polyclonal antibody.
Lane 1: GLRA1 transfected lysate(51.70 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — GLRA1
Entrez GeneID
2741GeneBank Accession#
BC074980Protein Accession#
NP_000162.2Gene Name
GLRA1
Gene Alias
MGC138878, MGC138879, STHE
Gene Description
glycine receptor, alpha 1
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene
Other Designations
OTTHUMP00000160616|glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome)|startle disease/hyperekplexia|stiff person syndrome
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Interactome
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Pathway
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Disease
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