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- Antibody Data
- Antigen structure
- References [8]
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- Product number
- ABIN350533 - Provider product page
- Provider
- antibodies-online
- Proper citation
- Antibodies-Online Cat#ABIN350533, RRID:AB_10785671
- Product name
- anti-G Protein-Coupled Receptor 143 (GPR143) (4th Cytoplasmic Domain) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide from the 4th cytoplasmic domain of human ocular albinism type 1 protein (G protein-coupled receptor 143 or GPR143, OA1) conjugated to an immunogenic carrier protein was used as the immunogen.
- Description
- Immunoaffinity chromatography
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- 4th Cytoplasmic Domain
- Vial size
- 100 μL
- Storage
- Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability.
- Handling
- Avoid freeze and thaw cycles.
Submitted references Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.
Proteomic analysis of early melanosomes: identification of novel melanosomal proteins.
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.
Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.
Ocular albinism: evidence for a defect in an intracellular signal transduction system.
OA1 mutations and deletions in X-linked ocular albinism.
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome.
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism.
Chi A, Valencia JC, Hu ZZ, Watabe H, Yamaguchi H, Mangini NJ, Huang H, Canfield VA, Cheng KC, Yang F, Abe R, Yamagishi S, Shabanowitz J, Hearing VJ, Wu C, Appella E, Hunt DF
Journal of proteome research 2006 Nov;5(11):3135-44
Journal of proteome research 2006 Nov;5(11):3135-44
Proteomic analysis of early melanosomes: identification of novel melanosomal proteins.
Basrur V, Yang F, Kushimoto T, Higashimoto Y, Yasumoto K, Valencia J, Muller J, Vieira WD, Watabe H, Shabanowitz J, Hearing VJ, Hunt DF, Appella E
Journal of proteome research 2003 Jan-Feb;2(1):69-79
Journal of proteome research 2003 Jan-Feb;2(1):69-79
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.
Bassi MT, Bergen AA, Bitoun P, Charles SJ, Clementi M, Gosselin R, Hurst J, Lewis RA, Lorenz B, Meitinger T, Messiaen L, Ramesar RS, Ballabio A, Schiaffino MV
Human genetics 2001 Jan;108(1):51-4
Human genetics 2001 Jan;108(1):51-4
Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.
Oetting WS, King RA
Human mutation 1999;13(2):99-115
Human mutation 1999;13(2):99-115
Ocular albinism: evidence for a defect in an intracellular signal transduction system.
Schiaffino MV, d'Addio M, Alloni A, Baschirotto C, Valetti C, Cortese K, Puri C, Bassi MT, Colla C, De Luca M, Tacchetti C, Ballabio A
Nature genetics 1999 Sep;23(1):108-12
Nature genetics 1999 Sep;23(1):108-12
OA1 mutations and deletions in X-linked ocular albinism.
Schnur RE, Gao M, Wick PA, Keller M, Benke PJ, Edwards MJ, Grix AW, Hockey A, Jung JH, Kidd KK, Kistenmacher M, Levin AV, Lewis RA, Musarella MA, Nowakowski RW, Orlow SJ, Pagon RS, Pillers DA, Punnett HH, Quinn GE, Tezcan K, Wagstaff J, Weleber RG
American journal of human genetics 1998 Apr;62(4):800-9
American journal of human genetics 1998 Apr;62(4):800-9
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome.
Bassi MT, Schiaffino MV, Renieri A, De Nigris F, Galli L, Bruttini M, Gebbia M, Bergen AA, Lewis RA, Ballabio A
Nature genetics 1995 May;10(1):13-9
Nature genetics 1995 May;10(1):13-9
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism.
Schiaffino MV, Bassi MT, Galli L, Renieri A, Bruttini M, De Nigris F, Bergen AA, Charles SJ, Yates JR, Meindl A
Human molecular genetics 1995 Dec;4(12):2319-25
Human molecular genetics 1995 Dec;4(12):2319-25
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