You are viewing an incomplete version of our website. Please click to reload the website as full version.

anti-Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND) Antibodies

BSND encodes an essential beta subunit for CLC chloride channels. Additionally we are shipping Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) Proteins (6) and Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) Kits (4) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
BSND 7809 Q8WZ55
BSND 140475 Q8VIM4
BSND 192675 Q8R2H3
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top anti-Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) Antibodies at antibodies-online.com

Showing 10 out of 45 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated IHC (p), WB Western blot analysis of BSND Antibody (C-term) (ABIN653815) in mouse liver tissue lysates (35 µg/lane). BSND (arrow) was detected using the purified polyclonal antibody. BSND Antibody (C-term) (ABIN653815) IHC analysis in formalin fixed and paraffin embedded mouse kidney tissue followed by peroxidase conjugation of the secondary antibody and DAB staining 400 μL Log in to see 10 to 11 Days
$324.50
Details
Human Rabbit Un-conjugated IHC (p), WB BSND Antibody (C-term) IHC analysis in formalin fixed and paraffin embedded mouse kidney tissue followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the BSND Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated. Western blot analysis of BSND Antibody (C-term) in mouse liver tissue lysates (35µg/lane). BSND (arrow) was detected using the purified Pab. 0.4 mL Log in to see 6 to 8 Days
$390.50
Details
Human Rabbit Un-conjugated WB WB Suggested Anti-BSND Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:62500Positive Control: Human heart WB Suggested Anti-BSND  Antibody Titration: 0.2-1 µg/mL ELISA Titer: 1:.2500  Positive Control: Human heart 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit PE IHC, ELISA, WB   200 μL Log in to see 8 to 10 Days
$969.83
Details
Human Rabbit Un-conjugated IP, WB 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) . Western Blot analysis of BSND expression in transfected 293T cell line by BSND MaxPab polyclonal antibody.Lane 1: BSND transfected lysate(35.20 KDa).Lane 2: Non-transfected lysate. 100 μL Log in to see 9 Days
$418.57
Details
Human Mouse Un-conjugated ELISA, WB Detection limit for recombinant GST tagged BSND is approximately 1ng/ml as a capture antibody. Western Blot detection against Immunogen (36.74 KDa) . 100 μg Log in to see 9 Days
$430.00
Details
Human Rabbit Un-conjugated IHC, WB   100 μL Log in to see 14 Days
$369.79
Details
Human Rabbit Un-conjugated ELISA   200 μL Log in to see 8 to 10 Days
$713.17
Details
Human Rabbit Un-conjugated WB Western Blot analysis of BSND expression in transfected 293T cell line by BSND MaxPab polyclonal antibody.Lane 1: BSND transfected lysate(35.20 KDa).Lane 2: Non-transfected lysate. 100 μg Log in to see 9 Days
$418.57
Details

BSND Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human , ,
,
,
, , , , ,
Mouse (Murine)


Rat (Rattus)


Top referenced anti-Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) Antibodies

  1. Human Polyclonal BSND Primary Antibody for IHC (p), WB - ABIN950606 : Riazuddin, Anwar, Fischer, Ahmed, Khan, Janssen, Zafar, Scholl, Husnain, Belyantseva, Friedman, Riazuddin, Friedman, Fahlke: Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. in American journal of human genetics 2009 (PubMed)
    Show all 5 references for ABIN950606

  2. Human Polyclonal BSND Primary Antibody for IHC (p), WB - ABIN653815 : Kathiresan, Willer, Peloso, Demissie, Musunuru, Schadt, Kaplan, Bennett, Li, Tanaka, Voight, Bonnycastle, Jackson, Crawford, Surti, Guiducci, Burtt, Parish, Clarke, Zelenika, Kubalanza, Morken, Scott, Stringham, Galan, Swift, Kuusisto, Bergman, Sundvall, : Common variants at 30 loci contribute to polygenic dyslipidemia. in Nature genetics 2008 (PubMed)
    Show all 2 references for ABIN653815

More Antibodies against Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) Interaction Partners

Human Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND) interaction partners

  1. results demonstrate that the carboxyl terminus of hClC-Kb is not part of the binding site for barttin, but functionally modifies the interplay with barttin.

  2. These results demonstrate that mutations in a cluster of hydrophobic residues within transmembrane domain 1 affect barttin-CLC-K (show CLCNKB Antibodies) interaction and impair gating modification by the accessory subunit

  3. R8W and G47R, two naturally occurring barttin mutations identified in patients with Bartter syndrome type IV, reduce barttin palmitoylation and CLC-K (show CLCNKB Antibodies)/barttin channel activity.

  4. BSND, was first modeled, and then, the identified mutation was further analyzed by using different bioinformatics tools.

  5. Case Report: G47R mutation decreases barttin expression, resulting CIC-K (show CLCNKB Antibodies) location being changed from the basement membrane to the cytoplasm in the tubule and might have varying effects on renal function associated with factors other than this gene.

  6. The mislocalization of CLC-K2 (show CLCNKB Antibodies) was identified as the molecular pathogenesis of Bartter syndrome by mutant barttins.

  7. ClC-Ka (show CLCNKB Antibodies)/barttin channels are regulated by SGK1 (show SGK1 Antibodies) and SGK3 (show SGK3 Antibodies), which may thus participate in the regulation of transport in kidney and inner ear.

  8. A missense, point mutation on gene BSND exon 1, affects the function of the CLC-K (show CLCNKB Antibodies)/barttin chloride channel (show CLCA1 Antibodies) and caused Bartter syndrome with sensorineural deafness in two families from Spain.

  9. Barttin mutations is associated with antenatal Bartter syndrome with sensorineural deafness

  10. Barttin modulates trafficking and function of ClC-K1 (show CLCNKA Antibodies) and ClC-Kb (show CLCNKB Antibodies) channels

Mouse (Murine) Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND) interaction partners

  1. induction of SGK1 (show SGK1 Antibodies), CLC-K1 (show CLCNKA Antibodies) and barttin by high osmolarity and change in intracellular volume in distal renal tubular cells in vivo and in vitro

  2. Bsnd(-/-) mice thus demonstrate a novel function of Cl(-) channels in generating the endocochlear potential and reveal the mechanism leading to deafness in human Bartter syndrome IV.

Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND) Antigen Profile

Protein 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.

Gene names and symbols associated with BSND

  • Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND) antibody
  • Bartter syndrome, infantile, with sensorineural deafness (Barttin) (Bsnd) antibody
  • BART antibody
  • BSND antibody
  • DFNB73 antibody

Protein level used designations for BSND

Bartter syndrome, infantile, with sensorineural deafness (Barttin) , barttin , deafness, autosomal recessive 73

GENE ID SPECIES
424663 Gallus gallus
615670 Bos taurus
740851 Pan troglodytes
100009026 Oryctolagus cuniculus
100173753 Pongo abelii
7809 Homo sapiens
140475 Mus musculus
192675 Rattus norvegicus
Selected quality suppliers for anti-Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND) Antibodies
Did you look for something else?