FAM108C1,FAM108C1蛋白抗体
英文名称: Anti-FAM108C1 antibody
型号:null    抗体货号: HZ-14692R
价格:请致电:010-57128832,18610462672
品牌: 中国/美国    产品商标: hzbscience

FAM108C1,FAM108C1蛋白抗体

产品编号HZ-14692R
英文名称FAM108C1
中文名称FAM108C1蛋白抗体
别 名abhydrolase domain containing 17C; Abhydrolase domain containing protein FAM108C1; Abhydrolase domain-containing protein FAM108C1; AB17C_HUMAN; FAM108C1; Family with sequence similarity 108 member C1.
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, Chicken, Pig, Cow,
FAM108C1,FAM108C1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 ICC=1:100-500 IF=1:100-500 (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36kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human FAM108C1
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.
FAM108C1,FAM108C1蛋白抗体PubMedPubMed
产品介绍background:
FAM108C1 is a 329 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding FAM108C1 maps to human chromosome 15, which encodes more than 700 genes and is made up of approximately 106 million base pairs. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Tissue Specificity:


Post-translational modifications:


Similarity:
Belongs to the AB hydrolase superfamily. FAM108 family.

Gene ID:
58489

FAM108C1,FAM108C1蛋白抗体Database links:
Entrez Gene: 58489 Human
Entrez Gene: 70178 Mouse
Entrez Gene: 361601 Rat
SwissProt: Q6PCB6 Human
SwissProt: Q8VCV1 Mouse
Unigene: 459072 Human
Unigene: 23914 Mouse
Unigene: 198511 Rat


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