PGM1 Antibody
-
中文名稱:PGM1兔多克隆抗體
-
貨號:CSB-PA017866HA01HU
-
規(guī)格:¥440
-
圖片:
-
Western blot
All lanes: PGM1 antibody at 6µg/ml
Lane 1: U251 whole cell lysate
Lane 2: U937 whole cell lysate
Lane 3: Jurkat whole cell lysate
Lane 4: Hela whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 62, 64, 41 kDa
Observed band size: 62 kDa -
Immunohistochemistry of paraffin-embedded human liver cancer using CSB-PA017866HA01HU at dilution of 1:100
-
Immunohistochemistry of paraffin-embedded human testis tissue using CSB-PA017866HA01HU at dilution of 1:100
-
Immunofluorescent analysis of HepG2 cells using CSB-PA017866HA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
-
-
其他:
產(chǎn)品詳情
-
產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) PGM1 Polyclonal antibody
-
Uniprot No.:
-
基因名:PGM1
-
別名:CDG1T antibody; Glucose phosphomutase 1 antibody; GSD14 antibody; OTTHUMP00000010519 antibody; OTTHUMP00000010520 antibody; PGM 1 antibody; PGM1 antibody; PGM1_HUMAN antibody; Phosphoglucomutase 1 antibody; Phosphoglucomutase-1 antibody; Phosphoglucomutase1 antibody
-
宿主:Rabbit
-
反應(yīng)種屬:Human
-
免疫原:Recombinant Human Phosphoglucomutase-1 protein (1-562AA)
-
免疫原種屬:Homo sapiens (Human)
-
標(biāo)記方式:Non-conjugated
本頁面中的產(chǎn)品,PGM1 Antibody (CSB-PA017866HA01HU),的標(biāo)記方式是Non-conjugated。對于PGM1 Antibody,我們還提供其他標(biāo)記。見下表:
-
克隆類型:Polyclonal
-
抗體亞型:IgG
-
純化方式:>95%, Protein G purified
-
濃度:It differs from different batches. Please contact us to confirm it.
-
保存緩沖液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
產(chǎn)品提供形式:Liquid
-
應(yīng)用范圍:ELISA, WB, IHC, IF
-
推薦稀釋比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:20-1:200 IF 1:50-1:200 -
Protocols:
-
儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
-
貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
-
用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關(guān)產(chǎn)品
靶點(diǎn)詳情
-
功能:This enzyme participates in both the breakdown and synthesis of glucose.
-
基因功能參考文獻(xiàn):
- PGM1 deficiency has been recognized as a cause of the congenital disorders of glycosylation. PMID: 29858906
- The structural perturbation resulting from mutation of this single amino acid reveals the molecular mechanism underlying PGM1 deficiency in these missense variants. PMID: 28117557
- Homozygous mutation in the PGM1 gene is associated with PGM1 deficiency. PMID: 26768186
- analysis of the structural basis of PGM1 enzyme dysfunction in PGM1 deficiency PMID: 26972339
- both PGM1 protein misfolding and catalytic impairment may play a role in PGM1 deficiency PMID: 25288802
- PGM1 is required for sustained cell growth during nutritional changes PMID: 24952355
- Phosphoglucomutase 1 deficiency, previously identified as a glycogenosis, is also a congenital disorder of glycosylation. PMID: 24499211
- The analysis involved the data on nine polymorphic codominant loci: HP, GC, TF, PI, PGM1, GLO1, C3, ACP1, and ESD. The loci were selected by significance of differences in genotype frequencies between tuberculosis patients and healthy controls PMID: 12942785
- Results report a novel human protein, calphoglin, which activates inorganic pyrophosphatase (IPP) and enhances phosphoglucomutase activity through the activated IPP. PMID: 15522220
- During extrauterine life, females carrying the PGM1*2 allele are relatively protected from extreme body mass increase, and during intrauterine life, PGM1*2/*2 homozygotes show a tendency to low body mass increase. PMID: 18091362
- There is a correlation between glomerular expression of MCP-1 and PGM1 and worsening renal prognosis in paediatric lupus nephritis. PMID: 18495743
- ZASP/Cypher anchors PGM1 to Z-disc under conditions of stress. The impaired binding of PGM1 to ZASP/Cypher might be involved in the pathogenesis of dilated cardiomyopathy. PMID: 19377068
顯示更多
收起更多
-
相關(guān)疾病:Congenital disorder of glycosylation 1T (CDG1T)
-
亞細(xì)胞定位:[Isoform 1]: Cytoplasm.
-
蛋白家族:Phosphohexose mutase family
-
數(shù)據(jù)庫鏈接: