7号染色体开放阅读框39抗体

¥1580 - 2480
gelatins
国内
2021-09-11 19:52

江西江蓝纯生物试剂有限公司

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江西江蓝纯生物试剂有限公司
夏丽
13524933993 021-54720761
3245176082@qq.com
产品属性
供应商江西江蓝纯生物试剂有限公司
数量137
克隆性单克隆
保质期1年
抗体英文名ZC3HAV1L/C7orf39
抗体名7号染色体开放阅读框39抗体
适应物种人/动物/植物
应用范围WB,ELISA等
浓度1mg/ml
保存条件-20 °
规格100ul/200ul
产品说明
产品货号 : jlcR18531
英文名称 : ZC3HAV1L/C7orf39
中文名称 : 7号染色体开放阅读框39抗体
:  B130055L09Rik; C7orf39; E430016P22Rik; RGD1309236; Zc3hav1l; ZCCHL_HUMAN; Zinc finger CCCH-type antiviral protein 1-like.
研究领域 : 神经生物学细胞膜受体表观遗传学
抗体来源 :  Rabbit
克隆类型 :  Polyclonal
交叉反应 : Human,
产品应用 :  ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 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.

:  33kDa
细胞定位 : 细胞浆
:  Lyophilized or Liquid
:  1mg/ml
:  KLH conjugated synthetic peptide derived from human ZC3HAV1L/C7orf39:201-300/300
:  IgG
纯化方法 :  affinity purified by Protein A
:  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.
PubMed : PubMed

产品介绍 : ZC3HAV1L is a 296 amino acid protein that contains two C3H1-type zinc fingers. Existing as two alternatively spliced isoforms, the gene encoding ZC3HAV1L maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

SWISS:
Q96H79

Gene ID:
92092

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

产品图片