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顶部产品介绍抗原信息化学信息储存和溶解信息计算器

Anti-CDMP1 Polyclonal Antibody

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货号 TMAB-04188

Anti-CDMP1 Polyclonal Antibody 是一种 Rabbit 抗体，靶向 CDMP1。Anti-CDMP1 Polyclonal Antibody 可用于 WB。

Anti-CDMP1 Polyclonal Antibody

Anti-CDMP1 Polyclonal Antibody

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Rating icon 还可以
货号 TMAB-04188

Anti-CDMP1 Polyclonal Antibody 是一种 Rabbit 抗体，靶向 CDMP1。Anti-CDMP1 Polyclonal Antibody 可用于 WB。

规格价格库存数量
50 μL
¥ 1,170
5日内发货
100 μL
¥ 1,960
5日内发货
200 μL
¥ 2,780
5日内发货
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产品介绍

生物活性
产品描述
Anti-CDMP1 Polyclonal Antibody is a Rabbit antibody targeting CDMP1. Anti-CDMP1 Polyclonal Antibody can be used in WB.
Ig Type
IgG
反应种属
Human,Mouse (predicted:Rat,Dog,Pig,Cow,Horse,Rabbit)
应用WB
推荐剂量
WB: 1:500-2000
抗体种类
Polyclonal
宿主来源Rabbit
亚细胞定位Secreted.
组织特异性Predominantly expressed in long bones during embryonic development.
构建方式Hybridoma Polyclonal Antibody
纯化方式Protein A purified
性状Liquid
缓冲液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
浓度1mg/ml
研究背景Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet. Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet. Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
抗原信息
免疫原
KLH conjugated synthetic peptide: human CDMP1/GDF5
抗原种属
Human
基因名称
GDF5
基因ID
8200
蛋白名称
Growth/differentiation factor 5
Uniprot ID
P43026
功能
Could be involved in bone and cartilage formation. Chondrogenic signaling is mediated by the high-affinity receptor BMPR1B.
化学信息
分子量Theoretical: 55 kDa.
储存&溶解度
储存方式Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
运输方式Shipping with blue ice.
存储store at low temperature | -20°C for 1 year

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