欢迎来到启研生物[ 会员登录 ] [ 立即注册 ]
400-812-0026

购物车0

您购物车为空,赶紧选购吧!
MATN3 Polyclonal Antibody
MATN3 Polyclonal Antibody
<
>
MATN3 Polyclonal Antibody
市场价格
经销商客户: ¥214.5
实验室客户: ¥292.5
近期销售量10 用户评价:comment rank 5()
文件与质量管理
浏览历史 [清空]

商品描述

商品属性

Target:MATN3

Gene Name:MATN3

Protein Name:Matrilin-3

Human Gene Id:4148

Human Swiss Prot No:O15232

Mouse Swiss Prot No:O35701

Immunogen:Synthesized peptide derived from part region of human protein

Specificity:MATN3 Polyclonal Antibody detects endogenous levels of protein.

Formulation:Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500-2000 ELISA 1:5000-20000

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Observed Band(KD):53kD

Background: This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains two von Willebrand factor A domains; it is present in the cartilage extracellular matrix and has a role in the development and homeostasis of cartilage and bone. Mutations in this gene result in multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008],

Function:disease:Defects in MATN3 are the cause of multiple epiphyseal dysplasia type 5 (EDM5) [MIM:607078]. EDM is a generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. EDM is broadly categorized into the more severe Fairbank and the milder Ribbing types. EDM5 is relatively mild and clinically variable. It is primarily characterized by delayed and irregular ossification of the epiphyses and early-onset osteoarthritis.,disease:Defects in MATN3 are the cause of spondyloepimetaphyseal dysplasia bowed-legs type (SEMD bowed-legs type) [MIM:608728]; also known as matrilin-3 related SEMD. Affected individuals show disproportionate early-onset dwarfism, bowing of the lower limbs, lumbar lordosis and normal hands. Skeletal abnormalities include short, wide and stocky long bones with s

Subcellular Location:Secreted .

Expression:Expressed only in cartilaginous tissues, such as vertebrae, ribs and shoulders.

广告说明