Anti-Collagen V/FITC Conjugated抗体
产品名称： Anti-Collagen V/FITC Conjugated抗体
英文名称： Anti-Collagen V/FITC
产品编号： YB--0552R-FITC
产品价格： null
产品产地： 中国/美国
品牌商标： Ybscience
更新时间： 2023-08-17T10:29:50
使用范围： 科研使用
上海钰博生物科技有限公司
- 联系人 : 陈环环
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- 邮编 : 200612
- 所在区域 : 上海
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- 邮箱 : shybio@126.com
Anti-Collagen V/FITC Conjugated抗体
| 产品编号 | YB-0552R-FITC |
| 英文名称 | Anti-Collagen V/FITC |
| 中文名称 | FITC标记的Ⅴ型胶原抗体 |
| 别 名 | Collagen Type V; AB collagen; Alpha 1 type V collagen; Alpha 2 type V collagen; Col5A1; Col5A2; COL5A2 protein; Col5A3; Collagen alpha 1(V) chain; Collagen alpha 2 (V) chain precursor; Collagen alpha 2(V) chain; Collagen alpha 3(V) chain; Collagen fetal membrane A polypeptide; Collagen type V alpha 1; Collagen type V alpha 2; Collagen type V alpha 3; Collagen V alpha 2 polypeptide; CollagenV; MGC105115; OTTHUMP00000064637; Pro alpha 1 type V collagen; Pro alpha 3(V) collagen; Procollagen alpha 2(V); Type V preprocollagen alpha 2 chain; collagen alpha-1(V) chain isoform 1 preproprotein. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 肿瘤 免疫学 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Rabbit, Sheep, |
| 产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 153kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human Collagen V |
| 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. |
| 产品介绍 | background: This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]. Function: Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin. Subunit: Trimers of two alpha 1(V) and one alpha 2(V) chains in most tissues and trimers of one alpha 1(V), one alpha 2(V), and one alpha 3(V) chains in placenta. Interacts with CSPG4. Subcellular Location: Secreted, extracellular space, extracellular matrix. Post-translational modifications: Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. Sulfated on 40% of tyrosines. DISEASE: Ehlers-Danlos syndrome 1 (EDS1) [MIM:130000]: A connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDS1 is the severe form of classic Ehlers-Danlos syndrome. Note=The disease is caused by mutations affecting the gene represented in this entry. Ehlers-Danlos syndrome 2 (EDS2) [MIM:130010]: Mild form of classic Ehlers-Danlos syndrome. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the fibrillar collagen family. Contains 1 fibrillar collagen NC1 domain. Contains 1 laminin G-like domain. Database links: Entrez Gene: 1289 Human Entrez Gene: 1290 Human Entrez Gene: 50509 Human Omim: 120190 Human Omim: 120215 Human Omim: 120216 Human SwissProt: P05997 Human SwissProt: P20908 Human SwissProt: P25940 Human SwissProt: Q15094 Human SwissProt: Q53WR4 Human SwissProt: Q5PR22 Human SwissProt: Q5SY11 Human SwissProt: Q86XF6 Human Unigene: 210283 Human Unigene: 235368 Human Unigene: 445827 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |