anti-Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9) 抗体

SLC7A9 encodes a protein that belongs to a family of light subunits of amino acid transporters. 再加上,我们可以发SLC7A9 试剂盒 (4)SLC7A9 蛋白 (4)和数多这个蛋白质的别的产品。

列出全部抗体 基因 基因ID UniProt
SLC7A9 11136 P82251
SLC7A9 116726 P82252
SLC7A9 30962 Q9QXA6
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产品编号 适用 宿主 标记 应用范围 图像 规格 交付 价格 详细
非结合性 IF (p), IHC (p), WB Antigen: 0.2 µg/100 µL  Primary: Antiserum, 1:500, 1:1000, 1:2000, 1:4000, 1:8000, 1:16000, 1:32000;  Secondary: HRP conjugated Goat-Anti-Rabbit IgG at 1: 5000;  TMB staining;  Read the data in MicroplateReader by 450 Formalin-fixed and paraffin embedded rat kidney labeled with Anti-SLC7A9 Polyclonal Antibody, Unconjugated  at 1:200 followed by conjugation to the secondary antibody and DAB staining 100 μL 14至21个工作日
$317.90
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非结合性 WB Western blot analysis of extracts of various cell lines, using SLC7A9 antibody. 200 μL 12至14个工作日
$438.90
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Cy5.5 IF (p)   100 μL 14至21个工作日
$416.90
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FITC IF (p)   100 μL 14至21个工作日
$416.90
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HRP IHC (p), WB   100 μL 14至21个工作日
$416.90
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Alexa Fluor 555 IF (p)   100 μL 14至21个工作日
$416.90
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Cy7 IF (p)   100 μL 14至21个工作日
$416.90
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Alexa Fluor 488 IF (p)   100 μL 14至21个工作日
$416.90
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Cy5 IF (p)   100 μL 14至21个工作日
$416.90
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Cy3 IF (p)   100 μL 14至21个工作日
$416.90
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引用最多的anti-SLC7A9 抗体

  1. Rat (Rattus) Polyclonal SLC7A9 Primary Antibody for IHC (fro), WB - ABIN549042 : Mizoguchi, Cha, Chairoungdua, Kim, Shigeta, Matsuo, Fukushima, Awa, Akakura, Goya, Ito, Endou, Kanai: Human cystinuria-related transporter: localization and functional characterization. in Kidney international 2001 (PubMed)
    Show all 2 Pubmed References

更多抗SLC7A9的相互作用对抗体

Human Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9) interaction partners

  1. Study shows that various computational tools were able to distinguish cystinuria-causing mutations from benign polymorphisms. Only missense mutation V142A had a benign effect on the protein structure and function of SLC7A9. The intron variant c.604+66C>G in SLC7A9 gene probably affected the splicing process.

  2. Thirteen pediatric patients with cystine stones were evaluated in our clinic between 2012 and 2015. Gene mutations in SLC3A1 and SLC7A9 were investigated

  3. Spectrum of SLC3A1 and SLC7A9 mutations in cystinuria patients presenting with prenatal hyperechoic colon has been described.

  4. Analysis showing how different mutations in SLC3A1 and SLC7A9 affect severity of cystinuria.

  5. A new variation in exon 4 of the SLC7A9 gene was identified in cystinuria patients, which was insertion of 1 adenine nucleotide between 2 cytosine nucleotides in position c.213-214insA.

  6. Five SLC3A1 and SLC7A9 mutations appear to be responsible for the genetic basis of cystinuria in the Greek-Cypriot patients

  7. G105R but not R333W mutation found in Iranian cystinuria patients

  8. Report no association of SLC7A9 mutations with clinical course of disease in cystinuria patients.

  9. Case Report: novel mutation of SLC7A9 gene in cystinuria.

  10. We present six family members with a complex phenotypic profile of cystinuria based on mutations in SLC3A1 (type A) or SLC7A9 (type B).

  11. In SLC7A9 gene, one large genomic rearrangement and 24 sequence variants are found in cystinuria patients.

  12. Studies identified 6 different alleles in SLC3A1 and 2 in SLC7A9 accounting for a total of 25 copy number changes, 11 in SLC3A1 and 14 in SLC7A9.

  13. a decreasing expression gradient of heterodimeric rBAT-b(0,+)AT along the proximal tubule is responsible for virtually all apical cystine reabsorption

  14. in cystinuria, the detection rate for mutations in SLC7A9 in children was 25% in the SLC7A9 gene for non-type I chromosomes.

  15. The finding of SLC7A9 mutations in all three subtypes underscores the complex interactions between specific cystinuria genes and other factors influencing cystine excretion.

  16. Three novel SLC7A9 mutations were identified: two missense mutations (P261L and V330M) and one single base-pair deletion (1009 delA)

  17. deletions in SLC7A9 in cystinuria

  18. Mutations of this protein have a population-specific distribution among south-east Europeans living in Germany.

  19. Mutational analysis should focus on this gene in inheritance of cytinuria.

  20. Disease: cystinuria, type non-I.Deletion codon 50.

Mouse (Murine) Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9) interaction partners

  1. a decreasing expression gradient of heterodimeric rBAT-b(0,+)AT along the proximal tubule is responsible for virtually all apical cystine reabsorption

  2. Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis

  3. mouse amino acid transport system B0 is a neutral amino acid transporter related to Hartnup disorder

  4. A new protocol with d-penicillamine to validate our Slc7a9 knockout mouse model for the study of the therapeutic effect of drugs in the treatment of cystine lithiasis is reported.

Pig (Porcine) Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9) interaction partners

  1. This study measured the intestinal expression of b(0,+)AT according to developmental stage, and documented the effect of intra-uterine growth restriction on such expression using real-time PCR and Western blot analysis.

  2. SLC7A9 mRNA was detected in brain, kidney, duodenum, jejunum, ileum, heart, liver, lung and muscle from Tibetan pigs

SLC7A9 抗原简介

蛋白简介

This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene.

Gene names and symbols associated with SLC7A9

  • solute carrier family 7 member 9 (SLC7A9) 抗体
  • solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 (slc7a9) 抗体
  • solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 L homeolog (slc7a9.L) 抗体
  • solute carrier family 7 member 9 (Slc7a9) 抗体
  • solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 (Slc7a9) 抗体
  • 4F2-LC6 抗体
  • BAT1 抗体
  • CSNU3 抗体

Protein level used designations for SLC7A9

solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 , B(0,+)-type amino acid transporter 1 , B(0,+)-type amino acid transporter 1-like , solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9 , b(0,+)AT , glycoprotein-associated amino acid transporter b0,+AT1 , solute carrier family 7 member 9 , b, + amino acid transporter , b, +AT , glycoprotein-associated amino acid transporter b0,+AT1 , amino acid transporter SLC7A9 b0,+AT , solute carrier family 7, member 9

GENE ID SPECIES
100056073 Equus caballus
415768 Gallus gallus
567117 Danio rerio
703081 Macaca mulatta
742762 Pan troglodytes
100013055 Monodelphis domestica
100127294 Xenopus laevis
100405463 Callithrix jacchus
100435972 Pongo abelii
100483798 Ailuropoda melanoleuca
100541772 Meleagris gallopavo
11136 Homo sapiens
116726 Rattus norvegicus
30962 Mus musculus
484601 Canis lupus familiaris
100037973 Sus scrofa
508174 Bos taurus
100008729 Oryctolagus cuniculus
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