SLC4A11 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of SLC4A11.
Immunogen
A synthetic peptide corresponding to C-terminus of human SLC4A11.
Host
Rabbit
Reactivity
Human, Mouse
Form
Liquid
Recommend Usage
ELISA (1:2000-1:5000)
Western Blot (1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (50% glycerol, 0.01% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot
Enzyme-linked Immunoabsorbent Assay
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Gene Info — SLC4A11
Entrez GeneID
83959Gene Name
SLC4A11
Gene Alias
BTR1, CDPD, CDPD1, CHED2, MGC126418, MGC126419, NABC1, dJ794I6.2
Gene Description
solute carrier family 4, sodium borate transporter, member 11
Gene Ontology
HyperlinkGene Summary
sodium borate transporter
Other Designations
OTTHUMP00000030097|bicarbonate transporter related protein 1|sodium-coupled borate cotransporter 1|solute carrier family 4 member 11|solute carrier family 4, sodium bicarbonate transporter-like, member 11
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Publication Reference
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SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T.
Human Molecular Genetics 2008 Mar; 17(5):656.
Application:WB-Tr, Human, HEK 293 cells.
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Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Desir J, Moya G, Reish O, Van Regemorter N, Deconinck H, David KL, Meire FM, Abramowicz MJ.
Journal of Medical Genetics 2007 May; 44(5):322.
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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
Jiao X, Sultana A, Garg P, Ramamurthy B, Vemuganti GK, Gangopadhyay N, Hejtmancik JF, Kannabiran C.
Journal of Medical Genetics 2007 Jan; 44(1):64.
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SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
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