ABIN350532

antibody from antibodies-online

Targeting: SH3GL2 CNSA2, EEN-B1, SH3D2A, SH3P4

Western blot (Recommended by provider)

Immunohistochemistry (Recommended by provider)

Antibody Data

Product number

ABIN350532

Provider

antibodies-online

Proper citation

Antibodies-Online Cat#ABIN350532, RRID:AB_10786658

Product name

anti-G Protein-Coupled Receptor 143 (GPR143) (Cytoplasmic Domain) antibody

Antibody type

Polyclonal

Antigen

A synthetic peptide from the 3d cytoplasmic domain of human GPR143 (OA1) conjugated to an immunogenic carrier protein was used as the antigen.

Description

Immunoaffinity chromatography

Reactivity

Human, Mouse, Rat

Host

Rabbit

Epitope

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.

References

Submitted references

Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.

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

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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

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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

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Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.

Oetting WS, King RA
Human mutation 1999;13(2):99-115

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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

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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

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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

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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