RFTN2,RFTN2蛋白抗体-抗体-抗体-生物在线
上海沪震实业有限公司
RFTN2,RFTN2蛋白抗体

RFTN2,RFTN2蛋白抗体

商家询价

产品名称: RFTN2,RFTN2蛋白抗体

英文名称: Anti-RFTN2 antibody

产品编号: HZ-8500R

产品价格: null

产品产地: 中国/美国

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: WB,ELISA,IHC-P,IHC-F,IF

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RFTN2,RFTN2蛋白抗体

产品编号HZ-8500R
英文名称RFTN2
中文名称RFTN2蛋白抗体
别 名Raft-linking protein 2; Raftlin-2; Rftn2; RFTN2_HUMAN.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Horse, Rabbit, Sheep,
RFTN2,RFTN2蛋白抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (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56kDa
细胞定位细胞膜
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human RFTN2
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 癈 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癈. 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 癈.
RFTN2,RFTN2蛋白抗体PubMedPubMed
产品介绍background:
Membrane microdomains known as lipid rafts are implicated in B-cell activation during B-cell receptor (BCR) signal initiation. Raftlin-2, also designated RFTN2 (raftlin family member 2) or raft-linking protein 2, is a 501 amino acid cell membrane protein that is essential for raft cell assembly and maintenance. A lipid anchor protein, Raftlin-2 belongs to the raftlin family and is encoded by a gene that maps to human chromosome 2q33.1 and mouse chromosome 1 C1.2. Human chromosome 2 is the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene.

Subcellular Location:
Cell membrane; Lipid-anchor (By similarity).

Similarity:
Belongs to the raftlin family.

RFTN2,RFTN2蛋白抗体Database links:
UniProtKB/Swiss-Prot: Q52LD8.3

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.