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產品詳情
  • 產品名稱:Anti-GLCNE抗體

  • 產品型號:GLCNE蛋白抗體
  • 產品廠商:KALANG
  • 產品文檔:
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簡單介紹:
Anti-GLCNE抗體產品質量穩定,實驗效果明顯,貨期快,價格優惠,歡迎垂詢訂購!我公司長期供應**組化抗體、WB抗體、**組化試劑盒和抗體試驗所需全部相關試劑、熒光標記抗體、單克隆抗體、多克隆抗體、各種標記的二抗IgG/IgM/IgD/IgA等科研實驗抗體。Anti-GLCNE抗體用于**組化實驗,WB實驗,相應的標記抗體有HRP標記抗體,FITC標記,BIO等。
詳情介紹:
Rabbit  Anti-GLCNE
Cat. Number:
Anti-GLCNE抗體KL-9882R
Quantity size:
0.2ml
Concentration:
1mg/ml   Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Background:
The bifunctional enzyme UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE/Mnk), or GLCNE, regulates and initiates biosynthesis of N-acetylneuraminic acid (NeuAc), a precursor of sialic acids. GLCNE is required for normal sialylation in hematopoietic cells. Sialylation is implicated in cell adhesion, signal transduction, tumorigenicity and metastatic behavior of malignant cells. It is upregulated Anti-GLCNE抗體after PKC-dependent phosphorylation and is most abundantly expressed in liver and placenta. It is also expressed, to a lesser extent, in heart, brain, lung, kidney, skeletal muscle and pancreas. Defects in GLCNE are the cause of sialuria, inclusion body myopathy 2 (IBM2) and Nonaka myopathy (NM) or distal myopathy with rimmed vacuoles (DMRV). Sialuria is an autosomal dominant disorder caused by a lack of feedback inhibition of GLCNE by CMP-NeuAc, resulting in overproduction of NeuAc. It is characterized by an accumulation of free sialic acid in the cytoplasm and large quantities of neuraminic acid in the urine. Both IBM2 and NM/DMRV are autosomal recessive neuromuscular disorders characterized by ***** onset, distal and proximal muscle weakness (especially in the legs) and a typical muscle pathology including filamentous inclusions and rimmed vacuoles.
Also known as:
IBM2; Uae1; Bifunctional UDP N Anti-GLCNE抗體acetylglucosamine 2 epimerase/N acetylmannosamine kinase; DMRV; ManAc kinase; N acylmannosamine kinase; NM; RP23-209M8.6; UDP GlcNAc 2 epimerase; UDP GlcNAc 2 epimerase/ManAc kinase; Uridine diphosphate N acetylglucosamine 2 epimerase; GLCNE_HUMAN.
Specificity:
Rabbit Polyclonal IgG, affinity purified by Protein A.
Reacts with: Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, Sheep, .
Immunogen: KLH conjugated synthetic peptide derived from human GLCNE.
Predicted Molecular Weight: 79kDa.Anti-GLCNE抗體
Storage:
Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).
Application:
WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  IF=1:50-200   
Not yet tested in other applications. Anti-GLCNE抗體
Optimal working dilutions must be determined by the end user.
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kl671Ra01 谷胱甘肽S轉移酶α3(GSTα3)多克隆抗體 Polyclonal Antibody to Glutathione S Transferase Alpha 3 (GSTa3)
kl672Hu01 Slit同源物2(Slit2)多克隆抗體 Polyclonal Antibody to Slit Homolog 2 (Slit2)
kl672Mu01 Slit同源物2(Slit2)多克隆抗體 Polyclonal Antibody to Slit Homolog 2 (Slit2)
kl672Ra01 Slit同源物2(Slit2)多克隆抗體 Polyclonal Antibody to Slit Homolog 2 (Slit2)
kl673Ca01 多巴胺受體D2(DRD2)多克隆抗體 Polyclonal Antibody to Dokline Receptor D2 (DRD2)
kl673Hu01 多巴胺受體D2(DRD2)多克隆抗體 Polyclonal Antibody to Dokline Receptor D2 (DRD2)
kl675Hu01 凝血因子Ⅴ(F5)多克隆抗體 Polyclonal Antibody to Coagulation Factor V (F5)
kl675Mu01 凝血因子Ⅴ(F5)多克隆抗體 Polyclonal Antibody to Coagulation Factor V (F5)
kl675Ra01 凝血因子Ⅴ(F5)多克隆抗體 Polyclonal Antibody to Coagulation Factor V (F5)
kl677Hu01 凝血因子Ⅻ(F12)多克隆抗體 Polyclonal Antibody to Coagulation Factor XII (F12)
kl677Mu01 凝血因子Ⅻ(F12)多克隆抗體 Polyclonal Antibody to Coagulation Factor XII (F12)
kl680Hu01 棕櫚酰化膜蛋白2(MPP2)多克隆抗體 Polyclonal Antibody to Membrane Protein, klmitoylated 2 (MPP2)
kl680Ra01 棕櫚酰化膜蛋白2(MPP2)多克隆抗體 Polyclonal Antibody to Membrane Protein, klmitoylated 2 (MPP2)
kl681Hu01 乙醇脫氫酶1(ADH1)多克隆抗體 Polyclonal Antibody to Alcohol Dehydrogenase 1 (ADH1)
kl681Mu01 乙醇脫氫酶1(ADH1)多克隆抗體 Polyclonal Antibody to Alcohol Dehydrogenase 1 (ADH1)
kl681Ra01 乙醇脫氫酶1(ADH1)多克隆抗體 Polyclonal Antibody to Alcohol Dehydrogenase 1 (ADH1)
kl683Hu01 Toll樣受體6(TLR6)多克隆抗體 Polyclonal Antibody to Toll Like Receptor 6 (TLR6)
kl685Hu01 CD14分子(CD14)多克隆抗體 Polyclonal Antibody to Cluster Of Differentiation 14 (CD14)

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