C1orf191,1号染色体开放阅读框191抗体
英文名称： Anti-C1orf191 antibody
型号:null    抗体货号： HZ-15050R
价格:请致电：010-57128832,18610462672
品牌: 中国/美国    产品商标: hzbscience

C1orf191,1号染色体开放阅读框191抗体

产品编号HZ-15050R
英文名称C1orf191
中文名称1号染色体开放阅读框191抗体
别 名Chromosome 1 open reading frame 191; MST128; MSTP128; Putative uncharacterized protein C1orf191; CA191_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,
C1orf191,1号染色体开放阅读框191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9kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C1orf191
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.
C1orf191,1号染色体开放阅读框191抗体PubMedPubMed
产品介绍Subcellular Location:
Secreted (Potential).

Database links:
Entrez Gene: 619518 Human
SwissProt: Q7Z2R9 Human
Unigene: 591438 Human


C1orf191,1号染色体开放阅读框191抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

RNA metabolism. It is essential for correct mitosis, and negatively regulates cell proliferation.

Subcellular Location:
Cytoplasm.

DISEASE:
Defects in DIS3L2 are the cause of Perlman syndrome (PRLMNS) [MIM:267000]. An autosomal recessive congenital overgrowth syndrome. Affected children are large at birth, are hypotonic, and show organomegaly, characteristic facial dysmorphisms (inverted V-shaped upper lip, prominent forehead, deep-set eyes, broad and flat nasal bridge, and low-set ears), renal anomalies (nephromegaly and hydronephrosis), frequent neurodevelopmental delay, and high neonatal mortality. Perlman syndrome is associated with a high risk of Wilms tumor. Histologic examination of the kidneys in affected children shows frequent nephroblastomatosis, which is a precursor lesion for Wilms tumor.

Similarity:
Belongs to the RNR ribonuclease family.

DIS3L2,有丝分裂控制蛋白样DIS3L2抗体Database links:
Entrez Gene: 129563 Human
Entrez Gene: 208718 Mouse
Entrez Gene: 367307 Rat
Omim: 614184 Human
SwissProt: Q8IYB7 Human
SwissProt: Q8CI75 Mouse
Unigene: 732236 Human
Unigene: 389152 Mouse
Unigene: 2940 Rat


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