SL9A3 Rabbit pAb ES9006
Specifications
| 50µl / 100µl |
Background:
SLC9A3 (Solute Carrier Family 9 Member A3) is a Protein Coding gene. Diseases associated with SLC9A3 include Diarrhea 8, Secretory Sodium, Congenital and Diarrhea 3, Secretory Sodium, Congenital, Syndromic. Among its related pathways are Collagen chain trimerization and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. he protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in SLC9A3 are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22.
Alternative names:
N/A
Clonality:
Polyclonal
Reactivity:
Human,Rat
Source:
Rabbit
Isotype:
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Immunogen:
Synthesized peptide derived from human protein . at AA range; 490-570
Concentration:
1mg/ml
Applications:
WB, ELISA
Recommende dilutions:
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Storage:
PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.
More info:
Email: info@sobekbio.com
Orders:
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