BSND MaxPab rabbit polyclonal antibody (D01)
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of BSND expression in transfected 293T cell line (H00007809-T01) by BSND MaxPab polyclonal antibody.
Lane 1: BSND transfected lysate(35.20 KDa).
Lane 2: Non-transfected lysate.
Immunoprecipitation
Immunoprecipitation of BSND transfected lysate using anti-BSND MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead, and immunoblotted with BSND purified MaxPab mouse polyclonal antibody (B01P) (H00007809-B01P).
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human BSND protein.
Immunogen
BSND (NP_476517.1, 1 a.a. ~ 320 a.a) full-length human protein.
Sequence
MADEKTFRIGFIVLGLFLLALGTFLMSHDRPQVYGTFYAMGSVMVIGGIIWSMCQCYPKITFVPADSDFQGILSPKAMGLLENGLAAEMKSPSPQPPYVRLWEEAAYDQSLPDFSHIQMKVMSYSEDHRSLLAPEMGQPKLGTSDGGEGGPGDVQAWMEAAVVIHKGSDESEGERRLTQSWPGPLACPQGPAPLASFQDDLDMDSSEGSSPNASPHDREEACSPQQEPQGCRCPLDRFQDFALIDAPTLEDEPQEGQQWEIALPNNWQRYPRTKVEEKEASDTGGEEPEKEEEDLYYGLPDGAGDLLPDKELGFEPDTQG
Host
Rabbit
Reactivity
Human
Interspecies Antigen Sequence
Mouse (70); Rat (71)
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.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of BSND expression in transfected 293T cell line (H00007809-T01) by BSND MaxPab polyclonal antibody.
Lane 1: BSND transfected lysate(35.20 KDa).
Lane 2: Non-transfected lysate.
Immunoprecipitation
Immunoprecipitation of BSND transfected lysate using anti-BSND MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead, and immunoblotted with BSND purified MaxPab mouse polyclonal antibody (B01P) (H00007809-B01P). -
Gene Info — BSND
Entrez GeneID
7809GeneBank Accession#
NM_057176.2Protein Accession#
NP_476517.1Gene Name
BSND
Gene Alias
BART, MGC119283, MGC119284, MGC119285
Gene Description
Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Gene Ontology
HyperlinkGene Summary
This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness. [provided by RefSeq
Other Designations
OTTHUMP00000009804|barttin
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Interactome
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Disease
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