产品货号:
Z25400
中文名称:
RIAM/APBB1IP抗体
英文名称:
Anti-RIAM/APBB1IP Antibody
产品规格:
50μl|100μl|150μl
发货周期:
1~3天
产品价格:
询价
抗体名称 | Anti-RIAM/APBB1IP Antibody |
指标别名 | APBB1 interacting protein 1;APBB1IP;INAG1;PREL 1;PREL1;Proline rich EVH1 ligand 1;Proline rich protein 73;RARP 1;RARP1;RIAM |
克隆性 | Polyclonal |
检验物种 | human,mouse,rat |
应用范围 | WB,IHC,IHC-F,ICC/IF,FCM |
基因名称 | APBB1IP |
抗体来源 | Rabbit |
抗体类型 | IgG |
免疫原 | A synthetic peptide corresponding to a sequence at the C-terminus of human APBB1IP(647-666aa EQDFMSDLMKALQKKRGNVS),different from the related rat sequence by one amino acid,and from the related mouse sequence by two amino acids. |
实际分子量 | 100KD |
成分 | 500μg/mL antibody with PBS,0.02% NaN3,1mg BSA and 50% glycerol. |
纯化方式 | Immunogen affinity purified. |
浓度 | 500μg/mL |
产品形态 | 溶液 |
保存条件 | 12 months from date of receipt,-20℃ as supplied.6 months 2 to 8℃ after reconstitution.Avoid repeated freezing and thawing. |
背景资料 | APBB1IP(APBB1-Interacting Protein),also called RIAM or RARP1,is a protein that in humans is encoded by the APBB1IP gene.By genomic sequence analysis,Lafuente et al.(2004) mapped the RIAM gene to chromosome 10p12.1.Using promoter-reporter gene assays,Inagaki et al.(2003) found that RARP1 suppressed transcription from AP1 and SRE sites,but not CRE sites,in all cell lines examined.The proline-rich regions of RARP1 suppressed AP1 transactivation.Lafuente et al.(2004) found that RIAM interacted with profilin and VASP,molecules that regulate actin dynamics,as well as with RAP1-GTP. |
Uniprot ID | Q7Z5R6 |
推荐配套试剂 | Biorab recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ZN1926) for Western blot,and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (ZN1865) for IHC(P).*Blocking peptide可以联系我们购买。 |
基因名全称 | amyloid beta(A4) precursor protein-binding,family B,member 1 interacting protein |
蛋白名全称 | Amyloid beta A4 precursor protein-binding family B member 1-interacting protein |
推荐稀释比 | Western blot(WB) 1:500~2000 Immunohistochemistry in paraffin section (IHC) 1:50~400 Immunohistochemistry in frozen section (IHC-F) 1:50~400 Immunocytochemistry/Immunofluorescence(ICC/IF) 1:50~400 Flow cytometry (FCM) 1~3μg/1×106 cells (Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
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