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RabbitAnti-Glypican 3 Recombinant Rabbit mAb  antibody (bsm-60006R)
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说明书: 50ul  100ul  
25ul/800.00元
50ul/1400.00元
100ul/2500.00元
大包装/询价

产品编号 bsm-60006R
英文名称 Glypican 3 Recombinant Rabbit mAb
中文名称 磷脂酰基醇蛋白聚糖-3重组兔单抗
别    名 GPC3; glypican3; glypican-3; Intestinal protein OCI-5; GTR2-2; MXR7.Intestinal protein OCI-5; GPC3_HUMAN.  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型
克 隆 号
交叉反应 Human, 
产品应用 WB=1:500-2000 Flow-Cyt=1:20-100 ICC=1:20-100 IF=1:20-100 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 65 kDa
检测分子量
细胞定位 细胞膜 细胞外基质 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 A synthesized peptide derived from human Glypican 3: 1-250/580 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

Function:
Cell surface proteoglycan that bears heparan sulfate. Inhibits the dipeptidyl peptidase activity of DPP4. May be involved in the suppression/modulation of growth in the predominantly mesodermal tissues and organs. May play a role in the modulation of IGF2 interactions with its receptor and thereby modulate its function. May regulate growth and tumor predisposition.

Subcellular Location:
Cell membrane and Secreted, extracellular space.

Tissue Specificity:
Highly expressed in lung, liver and kidney.

DISEASE:
Defects in GPC3 are the cause of Simpson-Golabi-Behmel syndrome type 1 (SGBS1) [MIM:312870]; also known as Simpson dysmorphia syndrome (SDYS). SGBS is a condition characterized by pre- and postnatal overgrowth (gigantism) with visceral and skeletal anomalies.

Similarity:
Belongs to the glypican family.

SWISS:
P51654

Gene ID:
2719

Database links:

Entrez Gene: 2719 Human

Entrez Gene: 14734 Mouse

Entrez Gene: 25236 Rat

Omim: 300037 Human

SwissProt: P51654 Human

SwissProt: Q8CFZ4 Mouse

SwissProt: P13265 Rat

Unigene: 644108 Human

Unigene: 22515 Mouse

Unigene: 9717 Rat



GPC-3磷脂酰基醇蛋白聚糖-3是一种硫酸类肝素蛋白多糖,GPC-3在不同的组织中具有不同的生物学功能,甚至起着完全不同的作用,可能与肿瘤组织类型、发病机制等密切相关.GPC3在绝大多数HCC(肝细胞癌)患者有表达。
产品图片
25 ug total protein per lane of various lysates (see on figure) probed with Glypican 3 monoclonal antibody, unconjugated (bsm-60006R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min.
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