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OA1 (K-16) 抗体: sc-47258

 |  说明书
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping near the N-terminus of OA1 of mouse origin
  • recommended for detection of OA1 of mouse origin by WB, IP, IF and ELISA
  • blocking peptide, sc-47258 P
 
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WB   IP   IF   siRNA  
 
种属 基因名称 基因ID 染色质位置 亚型(mRNA)即位号码 蛋白质即位号码 OMIM™ 号码
小鼠 Gpr143 18241 X F3 P70259
N/A
 
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产品名称产品编号规格价格数量添加我的最爱
OA1 (K-16) sc-47258 200 µg/ml $279
OA1 (K-16) P sc-47258 P
(peptide)
100 µg/0.5 ml $61
 siRNA 基因沉默子 (点击产品名称查看详细信息‭ ‬)
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OA1 siRNA (m) sc-61240 10 µM $258
OA1 (m)-PR sc-61240-PR 10 µM $23
 shRNA 质粒 (点击产品名称查看详细信息‭ ‬)
产品名称产品编号规格价格数量添加我的最爱
OA1 shRNA Plasmid (m) sc-61240-SH 20 µg $520
 shRNA 慢病毒颗粒 (点击产品名称查看详细信息‭ ‬)
产品名称产品编号规格价格数量添加我的最爱
OA1 shRNA (m) Lentiviral Particles sc-61240-V 200 µl $625

OA1 Background Information
G protein-coupled receptors (GPRs or GPCRs), are members of the largest protein family and play a role in many different stimulus-response pathways. G-protein coupled receptors mediate extracellular signals into intracellular signals (G-protein activation). They respond to a great variety of signaling molecules, including hormones, neurotransmitters and other proteins and peptides. GPR143, also designated ocular albinism type 1 protein (OA1), is detected exclusively in pigment cells. OA1, which is a multi-pass membrane protein, is a melanosomal protein expressed primarily in pigment cells. Defects in the gene encoding for OA1 cause ocular albinism, an X-linked disorder mainly characterized by retinal hypopigmentation and visual impairment.