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anti-Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) Antibodies

SLC4A11 encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Additionally we are shipping Solute Carrier Family 4, Sodium Borate Transporter, Member 11 Proteins (3) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
SLC4A11 311423  
SLC4A11 269356 A2AJN7
SLC4A11 83959 Q8NBS3
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Top anti-Solute Carrier Family 4, Sodium Borate Transporter, Member 11 Antibodies at antibodies-online.com

Showing 10 out of 30 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated ELISA, WB Western blot analysis of extracts from NIH-3T3/RAW264.7/A549 cells, using SLC4A11 Antibody. The lane on the right is treated with the synthesized peptide. 100 μg Log in to see 2 to 3 Days
$275.00
Details
Cow Goat Un-conjugated EIA, WB 0.1 mg Log in to see 6 to 8 Days
$379.50
Details
Human Goat Un-conjugated ELISA, WB 0.1 mg Log in to see 2 to 3 Days
$433.13
Details
Human Goat Un-conjugated IHC (p), ELISA, WB Human Kidney: Formalin-Fixed, Paraffin-Embedded (FFPE) 50 μg Log in to see 8 to 10 Days
$595.83
Details
Human Rabbit Un-conjugated ELISA, WB 100 μL Log in to see 8 to 10 Days
$478.50
Details
Human Rabbit Un-conjugated ELISA, WB   100 μg Log in to see 2 to 3 Days
$275.00
Details
Human Rabbit Un-conjugated ELISA, WB 100 μg Log in to see 11 to 16 Days
$412.86
Details
Human Rabbit Un-conjugated ELISA, WB 100 μL Log in to see 14 Days
$201.19
Details
Human Rabbit Un-conjugated IF (p), IHC (p), WB Formalin-fixed and paraffin embedded human kidney labeled with Anti-BT... 100 μL Log in to see 14 to 21 Days
$269.50
Details
Human Rabbit Un-conjugated IP   100 μL Log in to see 8 to 10 Days
$375.83
Details

SLC4A11 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Rat (Rattus) ,

Mouse (Murine) ,
,
Human , , , ,
,

Top referenced anti-Solute Carrier Family 4, Sodium Borate Transporter, Member 11 Antibodies

  1. Human Polyclonal SLC4A11 Primary Antibody for ELISA, WB - ABIN1535375 : Deloukas, Matthews, Ashurst, Burton, Gilbert, Jones, Stavrides, Almeida, Babbage, Bagguley, Bailey, Barlow, Bates, Beard, Beare, Beasley, Bird, Blakey, Bridgeman, Brown, Buck, Burrill, Butler, Carder et al.: The DNA sequence and comparative analysis of human chromosome 20. ... in Nature 2002 (PubMed)

  2. Cow (Bovine) Polyclonal SLC4A11 Primary Antibody for EIA, WB - ABIN487969 : Hemadevi, Veitia, Srinivasan, Arunkumar, Prajna, Lesaffre, Sundaresan: Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy. in Archives of ophthalmology 2008 (PubMed)

More Antibodies against Solute Carrier Family 4, Sodium Borate Transporter, Member 11 Interaction Partners

Xenopus laevis Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) interaction partners

Mouse (Murine) Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) interaction partners

  1. Successful knockout of the Slc4a11 gene was confirmed by immunohistochemistry and RT-PCR. Slit-lamp photography and AS-OCT (show Plxna2 Antibodies) showed progressive corneal edema.

  2. Loss of SLC4A11 leads to morphological changes in the fibrocytes and deafness.

  3. Results demonstrate the importance of NaBC1 (show BCAS1 Antibodies) in the audio-vestibular system and provide support for the hypothesis that SLC4A11 should be considered a potential candidate gene in patients with isolated sensorineural vestibular hearing abnormalities.

Human Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) interaction partners

  1. we report posterior polymorphous corneal dystrophy resulting from a de novo mutation in ZEB1 (show ZEB1 Antibodies). Additionally, we present a congenital hereditary endothelial dystrophy case with a thin Descemet membrane with a novel compound heterozygous SLC4A11 mutation.

  2. we review the current knowledge on the role of the SLC4A11 gene, protein, and its mutations in the pathophysiology and clinical presentation of CHED (show CDK13 Antibodies). [review]

  3. We report a novel nonsense mutation of the SLC4A11 gene in the patient with CHED2. In addition, one of heterozygous carriers in this family showed features of late onset Fuchs endothelial corneal dystrophy.

  4. SLC4A11 mutations contribute to 11% (5/45) of sporadic late-onset Late-onset Fuchs endothelial corneal dystrophy (FECD (show COL8a2 Antibodies)) in the cohort studied.

  5. SLC4A11 is a novel NH3/H+ co-transporter.

  6. We found that cells containing mutant SLC4A11 are more vulnerable to oxidative and mitochondrial damage, less able to overcome oxidative stress through the expression of sufficient levels of antioxidant genes, and are more prone to apoptotic death.

  7. In contrast to the Slc4a11(-/-) mouse, no abnormalities in daily renal ion excretion or polyuria were observed in the Harboyan syndrome patient.

  8. Potential therapeutic agents to improve the functional impairment of specific SLC4A11 mutant transporters.

  9. Our observations suggest that congenital hereditary endothelial dystrophy caused by homozygous SLC4A11 mutations progresses to Harboyan syndrome, but the severity of this may vary considerably.

  10. Variation in the COL8A2 (show COL8a2 Antibodies), SLC4A11, and ZEB1 (show ZEB1 Antibodies) genes is present in only a small fraction of African American cases and as such does not appear to significantly contribute to the genetic risk of Fuchs endothelial corneal dystrophy.

Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) Antigen Profile

Protein Summary

This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described.

Gene names and symbols associated with SLC4A11

  • solute carrier family 4, sodium borate transporter, member 11 (Slc4a11) antibody
  • solute carrier family 4, sodium borate transporter, member 11 (SLC4A11) antibody
  • solute carrier family 4, sodium borate transporter, member 11 (slc4a11) antibody
  • solute carrier family 4, sodium bicarbonate transporter-like, member 11 (Slc4a11) antibody
  • AI503023 antibody
  • BTR1 antibody
  • CDPD1 antibody
  • CHED2 antibody
  • dJ794I6.2 antibody
  • NABC1 antibody
  • si:dkey-12j14.4 antibody

Protein level used designations for SLC4A11

sodium bicarbonate transporter-like protein 11 , solute carrier family 4, sodium bicarbonate transporter-like, member 11 , solute carrier family 4, sodium borate transporter, member 11 , sodium-coupled borate transporter , sodium bicarbonate transporter-like protein 11-like , solute carrier family 4 member 11 , Sodium borate cotransporter 1 , Solute carrier family 4 member 11 , bicarbonate transporter-related protein 1 , bicarbonate transporter related protein 1 , sodium-coupled borate cotransporter 1

GENE ID SPECIES
311423 Rattus norvegicus
422943 Gallus gallus
485796 Canis lupus familiaris
532407 Bos taurus
718393 Macaca mulatta
100066656 Equus caballus
100157069 Sus scrofa
100219606 Taeniopygia guttata
100381166 Xenopus laevis
100406932 Callithrix jacchus
100444814 Pongo abelii
100486382 Xenopus (Silurana) tropicalis
458058 Pan troglodytes
559346 Danio rerio
100540067 Meleagris gallopavo
100580013 Nomascus leucogenys
269356 Mus musculus
83959 Homo sapiens
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