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LearnPAB16074
antibody from Abnova Corporation
Targeting: SLC4A11
BTR1, CDPD1, CHED2, dJ794I6.2, FECD4, NaBC1
Antibody data
- Antibody Data
- Antigen structure
- References [3]
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- Product number
- PAB16074 - Provider product page
- Provider
- Abnova Corporation
- Proper citation
- Abnova Corporation Cat#PAB16074, RRID:AB_10676562
- Product name
- SLC4A11 polyclonal antibody
- Antibody type
- Polyclonal
- Description
- Rabbit polyclonal antibody raised against synthetic peptide of SLC4A11.
- Storage
- Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Submitted references SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
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 1;17(5):656-66
Human molecular genetics 2008 Mar 1;17(5):656-66
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):322-6
Journal of medical genetics 2007 May;44(5):322-6
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):64-8
Journal of medical genetics 2007 Jan;44(1):64-8
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