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BMP-4 Monoclonal Antibody
商品货号: PLA004669
适 应 性:
WB ELISA
¥600元
规格:
在线咨询
MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: BMP4
  • 蛋白名称: Bone morphogenetic protein 4
  • Human_gene_id: 652
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=652
  • Human_swiss_prot_no: P12644
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P12644/entry
  • Mouse_swiss_prot_no: P21275
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P21275
  • 特异性: BMP-4 Monoclonal Antibody detects endogenous levels of BMP-4 protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
  • 纯化工艺: Affinity purification
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: BMP4; BMP2B; DVR4; Bone morphogenetic protein 4; BMP-4; Bone morphogenetic protein 2B; BMP-2B
  • 信号通路: Hedgehog;TGF-beta;Pathways in cancer;Basal cell carcinoma;
  • 功能: disease:Defects in BMP4 are the cause of microphthalmia syndromic type 6 (MCOPS6) [MIM:607932]; also known as microphthalmia and pituitary anomalies or microphthalmia with brain and digit developmental anomalies. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS6 is characterized by microphthalmia/anophthalmia associated with facial, genital, skeletal, neurologic and endocrine anomalies.,function:Induces cartilage and bone formation. Also act in mesoderm induction, tooth development, limb formation and fracture repair.,online information:Bone morphogenetic protein 4 entry,similarity:Belongs to the TGF-beta family.,subunit:Homodimer; disulfide-linked (By similarity). Interacts with GREM2 (By similarity) and SOSTDC1. Part of a complex consisting of TWSG1 and CHRD.,tissue specificity:Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Secreted, extracellular space, extracellular matrix.
  • 组织表达: Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines.
  • tag: hot
  • 科研货号: PLA004669
BMP-4 Monoclonal Antibody
Catalog No PLA004669
Product information
  • 发货日期: 7
  • 基因名称: BMP4
  • 蛋白名称: Bone morphogenetic protein 4
  • Human_gene_id: 652
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=652
  • Human_swiss_prot_no: P12644
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P12644/entry
  • Mouse_swiss_prot_no: P21275
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P21275
  • 特异性: BMP-4 Monoclonal Antibody detects endogenous levels of BMP-4 protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
  • 纯化工艺: Affinity purification
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: BMP4; BMP2B; DVR4; Bone morphogenetic protein 4; BMP-4; Bone morphogenetic protein 2B; BMP-2B
  • 信号通路: Hedgehog;TGF-beta;Pathways in cancer;Basal cell carcinoma;
  • 功能: disease:Defects in BMP4 are the cause of microphthalmia syndromic type 6 (MCOPS6) [MIM:607932]; also known as microphthalmia and pituitary anomalies or microphthalmia with brain and digit developmental anomalies. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS6 is characterized by microphthalmia/anophthalmia associated with facial, genital, skeletal, neurologic and endocrine anomalies.,function:Induces cartilage and bone formation. Also act in mesoderm induction, tooth development, limb formation and fracture repair.,online information:Bone morphogenetic protein 4 entry,similarity:Belongs to the TGF-beta family.,subunit:Homodimer; disulfide-linked (By similarity). Interacts with GREM2 (By similarity) and SOSTDC1. Part of a complex consisting of TWSG1 and CHRD.,tissue specificity:Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Secreted, extracellular space, extracellular matrix.
  • 组织表达: Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines.
  • tag: hot
  • 科研货号: PLA004669
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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