C15orf41,15号染色体开放阅读框41抗体

产品编号HZ-9619R
英文名称C15orf41
中文名称15号染色体开放阅读框41抗体
别 名Chromosome 15 open reading frame 41; CO041_HUMAN; HH114; Hypothetical protein LOC84529; Protein HH114; Uncharacterized protein C15orf41.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学 神经生物学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Chicken, Dog, Pig, Horse, Rabbit,
C15orf41,15号染色体开放阅读框41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32kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C15orf41
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.
C15orf41,15号染色体开放阅读框41抗体PubMedPubMed
产品介绍background:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. 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. The C15orf41 gene product has been provisionally designated C15orf41 pending further characterization.

Function:

DISEASE:

Gene ID:
84529

Database links:
Entrez Gene: 84529 Human
Entrez Gene: 399568 Mouse
SwissProt: Q9Y2V0 Human
SwissProt: Q3U4G0 Mouse
Unigene: 48348 Human
Unigene: 134929 Mouse

C15orf41,15号染色体开放阅读框41抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.