BSND monoclonal antibody (M01), clone 1E8

Catalog # H00007809-M01

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Size:100 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Sandwich ELISA (Recombinant protein)
Application

Sandwich ELISA (Recombinant protein)

Detection limit for recombinant GST tagged BSND is approximately 1ng/ml as a capture antibody.

QC Test

Western Blot detection against Immunogen (36.74 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant BSND.

    Immunogen

    BSND (NP_476517.1, 221 a.a. ~ 320 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    ACSPQQEPQGCRCPLDRFQDFALIDAPTLEDEPQEGQQWEIALPNNWQRYPRTKVEEKEASDTGGEEPEKEEEDLYYGLPDGAGDLLPDKELGFEPDTQG

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (60); Rat (61)

    Isotype

    IgG2b Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.74 KDa) .

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    Sandwich ELISA (Recombinant protein)

    Detection limit for recombinant GST tagged BSND is approximately 1ng/ml as a capture antibody.

    ELISA

  • Gene Info — BSND

    Entrez GeneID

    7809

    GeneBank Accession#

    NM_057176

    Protein Accession#

    NP_476517.1

    Gene Name

    BSND

    Gene Alias

    BART, MGC119283, MGC119284, MGC119285

    Gene Description

    Bartter syndrome, infantile, with sensorineural deafness (Barttin)

    Omim ID

    602522 606412

    Gene Ontology

    Hyperlink

    Gene 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

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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