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Product Name ALDOB Chinese Name 醛缩酶2抗体 Alias ALDB; ALDO B; ALDO2; ALDOB; ALDOB_HUMAN; Aldolase 2; Aldolase B; Aldolase B fructose bisphosphate; Aldolase2; AldolaseB; EC 4.1.2.13; Fructose bisphosphate aldolase B; Fructose-bisphosphate aldolase B; Liver type aldolase; Liver-type aldolase; MS1077. literatures Specific References (1) | SL4026R has been referenced in 1 publications.[IF=3.345] Xu et al. Morphological and proteomic analyses reveal that unsaturated guluronate oligosaccharide modulates multiple functional pathways in murine macrophage RAW264.7 cells. (2015) Mar.Drug. 13:1798-818 WB ; Mouse.Research Area Tumour Cell biology immunology Signal transduction transcriptional regulatory factor Immunogen Species Rabbit Clonality Polyclonal React Species Human, (predicted: Mouse, Rat, Pig, Cow, Rabbit, Sheep, ) Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 39kDa Cellular localization cytoplasmic Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human ALDOB: 261-364/364 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail ALDOB is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Defects in ALDOB cause hereditary fructose intolerance.
Subunit:
Homotetramer.
DISEASE:
Hereditary fructose intolerance (HFI) [MIM:229600]: Autosomal recessive disease that results in an inability to metabolize fructose and related sugars. Complete exclusion of fructose results in dramatic recovery; however, if not treated properly, HFI subjects suffer episodes of hypoglycemia, general ill condition, and risk of death the remainder of life. Note=The disease is caused by mutations affecting the gene represented in this entry.
Similarity:
Belongs to the class I fructose-bisphosphate aldolase family.
SWISS:
P05062
Gene ID:
229
Database links:Entrez Gene: 229 Human
Entrez Gene: 230163 Mouse
Omim: 612724 Human
SwissProt: P05062 Human
SwissProt: Q91Y97 Mouse
Unigene: 530274 Human
Unigene: 482116 Mouse
Unigene: 98207 Rat
醛缩酶(ALD)与机体能量代谢密切相关。醛缩酶含量比较丰富,分布也叫广泛,醛缩酶B是一种与糖酵解有关的酶类,在人类和哺乳动物组织中存在3种醛缩酶同工酶,即A(肌型),B(肝型)和C(脑型)。其中B型基因定位于q13-q32,属胞浆酶。研究表明,ALDOB在肝细胞癌发展过程中呈现出一定规律的变化,与原发性肝癌有关。ALDOB蛋白主要定位于胞浆。Product Picture
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