ABO Antibody, Biotin conjugated

說明書

中文名稱：

ABO兔多克隆抗體, Biotin偶聯
貨號：

CSB-PA001110LD01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) ABO Polyclonal antibody
Uniprot No.：

P16442
基因名：

ABO
別名：

ABO; Histo-blood group ABO system transferase; Fucosylglycoprotein 3-alpha-galactosyltransferase; Fucosylglycoprotein alpha-N-acetylgalactosaminyltransferase; Glycoprotein-fucosylgalactoside alpha-N-acetylgalactosaminyltransferase; Glycoprotein-fucosylgalactoside alpha-galactosyltransferase; Histo-blood group A transferase; A transferase; Histo-blood group B transferase; B transferase; NAGAT
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Histo-blood group ABO system transferase protein (235-354AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

Biotin
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
產品提供形式：

Liquid
應用范圍：

ELISA
Protocols：

ELISA Protocol
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.

產品評價

靶點詳情

功能：

This protein is the basis of the ABO blood group system. The histo-blood group ABO involves three carbohydrate antigens: A, B, and H. A, B, and AB individuals express a glycosyltransferase activity that converts the H antigen to the A antigen (by addition of UDP-GalNAc) or to the B antigen (by addition of UDP-Gal), whereas O individuals lack such activity.
基因功能參考文獻：
1. Conserved residues Arg188 and Asp302 are critical for active site organization and catalysis in human ABO(H) blood group A and B glycosyltransferases. PMID: 29873711
2. rs579459 and rs505922 within ABO gene and their interaction are associated with increased ischemic stroke risk in Chinese population PMID: 28984382
3. These data suggest that single nucleotide polymorphisms ABO rs8176719 and FGG rs2066865 may contribute individually to the venous thromboembolism susceptibility in the Portuguese population. PMID: 29995659
4. Bm5.8 deletion is a predominant allele accounting for 99.77% of the Bm alleles in the Japanese individuals with Bm and A1Bm phenotypes. PMID: 29473176
5. A rare novel B allele was identified in a B variant. The mutation 518T > C may decrease the glycosyltransferase enzymatic activity and result in the weak B variant, with the presence of anti-B in serum. PMID: 29106707
6. The data indicated that the transcription levels of the ABO gene changed with acute myeloid leukemia (AML) disease progression, suggesting its potential role in the progression of AML disease. PMID: 28939368
7. the genetic variants in ABO gene may influence the risk of large artery atherosclerotic stroke in Chinese Han population. PMID: 26924317
8. A Korean man and his two sons had an ABO mutation at nucleotide position 721 (C substituted by G), resulting in an amino acid change from arginine to glycine. This mutation may affect enzyme activity and/or protein expression. PMID: 28833251
9. Kinetic analysis of GTA and GTB point mutants E303C, E303D, E303Q and E303A shows that despite the enzymes having nearly identical sequences, the corresponding mutants of GTA/GTB have up to a 13-fold difference in their residual activities relative to wild type PMID: 27979997
10. an ABO exonic missense mutation affects B-antigen expression by decreasing the mRNA level of the ABO gene PMID: 28653406
11. Binding either of the donor substrate UDP-Gal or of UDP induces a semiclosed conformation of blood group glycosyltransferases A and B. PMID: 28256109
12. These results support the contention that ABO expression is dependent upon a downstream positive regulatory element functioning through a tissue-restricted transcription factor, Elf5, in epithelial cells. PMID: 27587399
13. The Arg180 residue in the loop region of the ABO glycosyltransferases structure plays significant role in stabilizing its closed conformation. PMID: 27538125
14. Our findings indicated that genetic variations of ABO gene may contribute to susceptibility of large artery atherosclerosis but not ischemic stroke and small vessel diseases in the Chinese population PMID: 27542834
15. High Blood type A, is associated with recurrence in bladder cancer among patients undergoing radical cystectomy. PMID: 26329815
16. Data suggest women with blood groups A, B, O (i.e. non-AB) exhibit increased risk for gestational diabetes mellitus (GDM) compared with those with blood group AB; thus, glycosylation of the H antigen via NAGAT may be risk/protective factor for GDM. PMID: 25820620
17. We validated a strong influence of ABO blood type on von Willebrand Factor levels, but also detected a direct ABO influence on FVIII activity and FVIII/VWF ratio after adjustment for VWF. PMID: 26244499
18. AQP1 and ABO variants appear to predict hemoglobin and hematocrit levels but not other erythrocyte phenotype parameters including red blood cell counts and red blood cell indices PMID: 26632894
19. No association was found between FUT2 and ABO single nucleotide polymorphism (SNPs) and chronic pancreatitis. PMID: 25814649
20. this study documented down-regulation of galectin-3 and Bcl-2 (antiapoptotic molecules) and stepwise increase of survivin (inhibitor of apoptosis), during thyroid tumor progression from PTC to ATC. PMID: 25471003
21. Non-O blood type is associated with future cardiovascular events in Chinese Han patients undergoing coronary angiography. PMID: 26512559
22. Blood group A and genotype AA showed the highest risks of hepatocellular carcinoma. PMID: 25854361
23. An association between blood type O and the occurrence of neuroendocrine tumors in MEN1 patients was not confirmed. PMID: 26247473
24. ABO blood type was not associated with risk of aggressive prostate cancer. PMID: 26268879
25. This study provided evidence of SNP rs505922 C allele of the ABO gene as a strong risk factor of cancer susceptibility, specifically for pancreatic cancer. PMID: 25656610
26. Alteration of DNA sequence in the ABO gene resulted in amino acid substitutions and led to a weak or missing expression of ABO antigens. PMID: 25217989
27. The FII G19911A and FII C20068T are potentially associated with an increased risk for the occurrence of isolated pulmonary embolism PMID: 26148378
28. alpha 1-3-N-acetylgalactosaminyltransferase-knockout pig did not appear to have an advantage over the GalT-KO pig with respect to reactivity with human antibodies from a xenotransplantation perspective PMID: 24219248
29. The catalytic mechanism of the human alpha-(1,3)-galactosyltransferase (GTBWT) and its E303C mutant (GTBE303C) has been described. PMID: 25138306
30. Eight heterozygous sites in exons 6 and 7 (261delG 297A/G, 421C/T, 467C/T, 646T/A, 681G/A, 771C/T, 829G/A) of the ABO gene were identified PMID: 25636112
31. We unraveled a novel A(weak) allele (ABO*AW.29) in a case of apparent nonmaternity PMID: 25156869
32. Data indicate that mong 7111 tested ABO blood-group system gene, 75 were assigned as A2 or A2B phenotypes. PMID: 25297604
33. The rs495828 polymorphism of the ABO gene was associated with enalapril-induced cough and may serve as a useful pharmacogenomics marker of the safety of enalapril in Chinese patients with essential hypertension. PMID: 24743543
34. the GWAS-identified ABO variants (rs505922, rs495828, rs657152, and rs630014) were found to be associated with risk of pancreatic ductal adenocarcinoma in a Chinese population PMID: 23816557
35. Nucleotide substitutions in transcriptional regulatory elements in the ABO promoter, decrease transcription from the A- and B-alleles, resulting in reduction in A- and B-antigen expression in A3 and B3, respectively. PMID: 24602004
36. The sequence of alpha 1,3 galactosyltransferase B allele has differed from that of regular B101 allele. PMID: 24510570
37. Twenty-nine ABO subgroup alleles were newly linked to different kinds of ABO variations. We provide the first evidence that promoter abnormality is involved in the formation of weak ABO phenotypes. PMID: 23521133
38. the mutation in the GATA motif of the erythroid-specific regulatory element may diminish the binding of GATA transcription factors and down regulate transcriptional activity of the element on the B allele. PMID: 23560502
39. High cholesterol absorption is associated with risk alleles in ABO (and ABCG8) and with cardiovascular disease. PMID: 23707316
40. A novel A allele with the 595C >T mutation identified in a Chinese individual with the Am phenotype. PMID: 23387832
41. Single-nucleotide polymorphisms in ABO gene is associated with variation in soluble E-selectin levels leading to cardiovascular diseases. PMID: 23300549
42. SNPs in the ABO gene are associated with risk of advanced precancerous gastric lesions in individuals infected with Helicobacter pylori, dependent on cagA status PMID: 23319424
43. Patients with ABO blood group genetic mutation are at risk developing venous thromboembolism and myocardial infarction. PMID: 23382263
44. ABO genetic variants are associated with large-vessel and cardioembolic stroke but not small-vessel disease. PMID: 23381943
45. Linkage analysis identifies an ABO locus on chromosome 9q34 for plasma von Willebrand factor that explained 24.5% of the variance in VWF levels. PMID: 23267103
46. Our findings confirm that ABO is one of the genetic factors that are associated with hematological traits in the Korean population. PMID: 22963146
47. Compared to group A/non-secretors, group O/non-secretor individuals were at increased risk of carrying S. aureus in their throat.Histo-blood group antigens appear to act as ligands for S. aureus and may contribute to the observed population variation in pharyngeal S. aureus colonization. PMID: 22664149
48. The minor allele of rs505922 and the resulting non-O blood types are not associated with increased risk or less favorable tumor characteristics or prognosis in breast cancer. PMID: 22642827
49. A common variant of the ABO gene protects against hypertension in a Spanish population. PMID: 22258027
50. Genetic variations at the ABO locus are associated with circulating levels of ICAM1, P-selectin, and E-selectin. PMID: 22010135
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亞細胞定位：

Golgi apparatus, Golgi stack membrane; Single-pass type II membrane protein. Secreted. Note=Membrane-bound form in trans cisternae of Golgi. Secreted into the body fluid.
蛋白家族：

Glycosyltransferase 6 family
數據庫鏈接：

HGNC: 79

OMIM: 110300

KEGG: hsa:28

UniGene: Hs.654423

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