产品简要
公司名称 :
MyBioSource
产品类型 :
抗体
产品名称 :
Polyclonal Antibody to Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2)
目录 :
MBS2028051
规格 :
0.01毫克
价格 :
110美元
克隆性 :
多克隆
宿主 :
共轭标签 :
未共轭
反应物种 :
人类
应用 :
免疫印迹, 免疫组化, 免疫细胞化学, 免疫沉淀
更多信息或购买 :
图像
图像 1 :
MyBioSource MBS2028051 图像 1
Western Blot; Sample: Human Hela cell lysate;. Primary Ab: 1µg/ml Rabbit Anti-Human ROR2 Antibody. Second Ab: 0.2µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody. (Catalog: MBS2086047)
图像 2 :
MyBioSource MBS2028051 图像 2
Western Blot;. Sample: Recombinant ROR2, Human.
图像 3 :
MyBioSource MBS2028051 图像 3
DAB staining on IHC-P; Samples: Human Stomach Tissue;. Primary Ab: 20ug/ml Rabbit Anti-Human ROR2 Antibody Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody (Catalog: MBS2086047)
产品信息
目录号 :
MBS2028051
产品类型 :
抗体
产品全称 :
Polyclonal Antibody to Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2)
产品简称 :
[Receptor Tyrosine Kinase Like Orphan Receptor 2]
其他名称 :
[tyrosine-protein kinase transmembrane receptor ROR2 isoform 2; Tyrosine-protein kinase transmembrane receptor ROR2; tyrosine-protein kinase transmembrane receptor ROR2; receptor tyrosine kinase like orphan receptor 2; Neurotrophic tyrosine kinase, receptor-related 2]
产品基因名称 :
[ROR2]
其他基因名称 :
[ROR2;ROR2;BDB;BDB1;NTRKR2;NTRKR2]
克隆性 :
多克隆
宿主 :
纯度 :
Antigen-specific affinity chromatography followed by Protein A affinity chromatography
形式 :
Supplied as solution form in PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
浓度 :
0.35毫克/毫升
储存稳定性 :
Storage: Avoid repeated freeze/thaw cycles. Store at 4ºC for frequent use. Aliquot and store at -20ºC for 12 months. Stability Test: The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
检测过的应用 :
免疫印迹(免疫印迹), 免疫组化(免疫组化), 免疫细胞化学(免疫细胞化学), 免疫沉淀(免疫沉淀)
应用笔记 :
Western blotting: 0.5-2 ug/mL;1:170-700. Immunohistochemistry: 5-20 ug/mL;1:17-70. Immunocytochemistry: 5-20 ug/mL;1:17-70. Optimal working dilutions must be determined by end user
image1头 :
免疫印迹(免疫印迹)
image2头 :
免疫印迹(免疫印迹)
image3头 :
免疫组化(免疫组化)
其它信息1 :
Organism Species: Homo sapiens (Human). Source: Polyclonal antibody preparation. Traits: Liquid. Immunogen: Recombinant ROR2 (Trp683~Val934) expressed in E.coli
其他信息2 :
Conjugate: No Conjugate. Immunogen: Recombinant ROR2 (Trp683~Val934) expressed in E Coli. Conjugated Antibody: The APC conjugated antibody version of this item is also available as catalog #MBS2074331
NCBI GI登录号 :
970598266
NCBI登录号 :
NP_001305133.1
NCBI基因登录号 :
NM_001318204.1
UniProt数据库登录号 :
Q01974
NCBI信号通路 :
Beta-catenin Independent WNT Signaling Pathway (1269610); Cardiac Progenitor Differentiation Pathway (712094); Noncanonical Wnt Signaling Pathway (169354); PCP/CE Pathway (1269611); Signal Transduction Pathway (1269379); Signaling By Wnt Pathway (1269594); WNT5A-dependent Internalization Of FZD2, FZD5 And ROR2 Pathway (1269614); Wnt Signaling Pathway NetPath (198799); Wnt Signaling Network Pathway (137962)
NCBI总结 :
The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]
UniProt数据库总结 :
ROR2: a receptor tyrosine kinase of the ROR family. May be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. Protein type: EC 2.7.10.1; Kinase, protein; Membrane protein, integral; Protein kinase, TK; Protein kinase, tyrosine (receptor); Ror family; TK group. Chromosomal Location of Human Ortholog: 9q22.31. Cellular Component: cell soma; cell surface; dendrite; integral component of plasma membrane; microtubule; plasma membrane. Molecular Function: ATP binding; coreceptor activity involved in Wnt signaling pathway, planar cell polarity pathway; frizzled binding; metal ion binding; protein binding; transmembrane receptor protein tyrosine kinase activity; Wnt-protein binding. Biological Process: astrocyte development; BMP signaling pathway; bone mineralization; cartilage condensation; cell fate commitment; embryonic digit morphogenesis; embryonic genitalia morphogenesis; inner ear morphogenesis; JNK cascade; macrophage migration; male genitalia development; multicellular organism development; negative regulation of canonical Wnt signaling pathway; negative regulation of cell proliferation; peptidyl-tyrosine phosphorylation; positive regulation of canonical Wnt signaling pathway; positive regulation of cell migration; positive regulation of JUN kinase activity; positive regulation of macrophage differentiation; positive regulation of protein kinase C activity; positive regulation of synaptic transmission, glutamatergic; positive regulation of transcription, DNA-templated; signal transduction; smoothened signaling pathway; somitogenesis; transmembrane receptor protein tyrosine kinase signaling pathway; Wnt receptor signaling pathway, calcium modulating pathway; Wnt receptor signaling pathway, planar cell polarity pathway. Disease: Brachydactyly, Type B1; Robinow Syndrome, Autosomal Recessive
尺寸1 :
0.01毫克
价格1 :
110美元
尺寸2 :
0.02毫克
价格2 :
130
size3 :
0.05毫克
价格3 :
175
size4 :
0.1毫克
price4 :
225
size5 :
0.2毫克
price5 :
340
size6 :
1毫克
price6 :
800
更多信息或购买 :
公司信息
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-858-633-0165
公司总部: 美国
MyBioSource,LLC最初由三名热情澎湃的提供高品质试剂的科学家联合创立于温哥华,公司愿景是“生物研究试剂的源头”,现在位于圣地亚哥市。