This fast track antibody is not yet fully characterized. It is subject to these
terms and conditions
概述
-
产品名称Anti-Collagen XI alpha 2抗体
参阅全部 Collagen XI alpha 2 一抗 -
描述山羊多克隆抗体to Collagen XI alpha 2
This product is a fast track antibody. It has been affinity purified and shows high titre values against the immunizing peptide by ELISA. Read the terms of use »
-
特异性This antibody is expected to recognise all three reported isoforms (NP_542411.1; NP_542412.1; NP_542410.1).
-
种属反应性
预测可用于: Human
-
免疫原
Synthetic peptide:
QKELECEGGQRERPQ
, corresponding to Internal sequence amino acids 223-237 of Human Collagen XI alpha 2
性能
-
形式Liquid
-
存放说明Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
-
存储溶液Preservative: 0.02% Sodium Azide
Constituents: 0.5% BSA, Tris saline, pH 7.3 -
Concentration information loading... -
纯度Immunogen affinity purified
-
纯化说明Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
-
克隆多克隆
-
同种型IgG
-
研究领域
相关产品
-
Compatible Secondaries
应用
应用说明
This antibody gave a positive result in ELISA against the immunizing peptide. Antibody detection limit dilution 1:1,000.
Western Blot: Preliminary experiments in Human Brain and Bone Marrow lysates gave no specific signal but low background (at antibody concentration up to 1ug/ml).
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Western Blot: Preliminary experiments in Human Brain and Bone Marrow lysates gave no specific signal but low background (at antibody concentration up to 1ug/ml).
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
靶标
-
功能May play an important role in fibrillogenesis by controlling lateral growth of collagen II fibrils.
-
疾病相关Defects in COL11A2 are the cause of Stickler syndrome type 3 (STL3) [MIM:184840]. STL3 is an autosomal dominant non-ocular form of Stickler syndrome. Classical Stickler syndrome associates ocular signs with more or less complete forms of Pierre Robin sequence, bone disorders and sensorineural deafness. Ocular symptoms are absent in STL3. Robin sequence includes an opening in the roof of the mouth (a cleft palate), a large tongue (macroglossia), and a small lower jaw (micrognathia). Bones are affected by slight platyspondylisis and large, often defective epiphyses. Juvenile joint laxity is followed by early signs of arthrosis. The degree of hearing loss varies among affected individuals and may become more severe over time. Syndrome expressivity is variable.
Defects in COL11A2 are the cause of autosomal recessive otospondylomegaepiphyseal dysplasia (OSMED) [MIM:215150]. OSMED is a skeletal dysplasia accompanied by severe hearing loss. The phenotype overlaps that of autosomal dominant skeletal disorders (Stickler and Marshall syndromes) but can be distinguished by disproportionately short limbs and lack of ocular involvement.
Defects in COL11A2 are the cause of Weissenbacher-Zweymueller syndrome (WZS) [MIM:277610]. WZS is an autosomal dominant disorder allelic with STL3 and OSMED. WZS is also referred to as heterozygous OSMED.
Defects in COL11A2 are the cause of deafness autosomal dominant type 13 (DFNA13) [MIM:601868]. DFNA13 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
Defects in COL11A2 are the cause of deafness autosomal recessive type 53 (DFNB53) [MIM:609706]. -
序列相似性Belongs to the fibrillar collagen family.
Contains 1 fibrillar collagen NC1 domain.
Contains 1 TSP N-terminal (TSPN) domain. -
翻译后修饰Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.
A disulfide-bonded peptide called proline/arginine-rich protein or PARP is released from the N-terminus during extracellular processing and is subsequently retained in the cartilage matrix from which it can be isolated in significant amounts. -
细胞定位Secreted > extracellular space > extracellular matrix.
- Information by UniProt
-
数据库链接
- Entrez Gene: 1302 Human
- Omim: 120290 Human
- SwissProt: P13942 Human
- Unigene: 390171 Human
-
别名
- COBA2_HUMAN antibody
- COL11A2 antibody
- Collagen alpha 2(XI) antibody
see all
Anti-Collagen XI alpha 2 antibody (ab42708)参考文献
ab42708 has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"