微原纤维胶原相关蛋白1抗体_价格_上海联迈生物工程有限公司

产品详情

微原纤维胶原相关蛋白1抗体

英文名称 MFAP1

中文名称微原纤维胶原相关蛋白1抗体

别名 MFAP1 is an extracellular protein associated with elastic fiber microfibrils.

研究领域细胞生物信号转导细胞周期蛋白细胞骨架细胞外基质

抗体来源 Rabbit

克隆类型 Polyclonal

交叉反应 Human, Mouse, Rat, Chicken, Pig, Cow,

产品应用 WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.

分子量 52kDa

细胞定位细胞外基质分泌型蛋白

性状 Lyophilized or Liquid

浓度 1mg/ml

免疫原 KLH conjugated synthetic peptide derived from human MFAP1:31-120/439

亚型 IgG

纯化方法 affinity purified by Protein A

储存液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed PubMed

产品介绍 Microfibrils are an important component of the extracellular matrix of many tissues and can either associate with or without elastin. Several microfibril associated proteins (MFAPs) have been cloned, including MFAP1, MFAP3 and MFAP4. The MFAP1 and MFAP3 genes are localized near the fibrillin genes FBN1 and FBN2, respectively. Mutations in FBN1 are linked to Marfan syndrome. Mutations in FBN2 have been linked to congenital contractural arachnodactyly. This suggests roles for MFAP1 and MFAP3 in heritable diseases affecting microfibrils. Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS), a clinically recognizable multiple congenital anomaly/mental retardation syndrome.

微原纤维胶原相关蛋白1抗体信息由上海联迈生物工程有限公司为您提供，如您想了解更多关于微原纤维胶原相关蛋白1抗体报价、型号、参数等信息，欢迎来电或留言咨询。除供应微原纤维胶原相关蛋白1抗体外，上海联迈生物工程有限公司还可为您提供调亡诱导因子抗体、磷酸化CREB-1抗体等产品，公司有专业的客户服务团队，是您值得信赖的合作伙伴。

供货周期：	现货
品牌：	LMAI Bio
规格：	50ul/100ul/200ul
货号：	LM7810R
CAS号：