GMPPB Antibody

中文名稱：

GMPPB兔多克隆抗體
貨號：

CSB-PA896740LA01HU
規(guī)格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human prostate cancer using CSB-PA896740LA01HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human adrenal gland tissue using CSB-PA896740LA01HU at dilution of 1:100
其他：

產(chǎn)品詳情
產(chǎn)品評價
相關產(chǎn)品
靶點詳情

產(chǎn)品詳情

產(chǎn)品名稱：

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

Q9Y5P6
基因名：

GMPPB
別名：

GDP mannose pyrophosphorylase B antibody; GDP-mannose pyrophosphorylase B antibody; GMPPB antibody; GMPPB_HUMAN antibody; GTP-mannose-1-phosphate guanylyltransferase beta antibody; KIAA1851 antibody; Mannose 1 phosphate guanylyltransferase antibody; Mannose-1-phosphate guanyltransferase beta antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Mannose-1-phosphate guanyltransferase beta protein (61-360AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產(chǎn)品，GMPPB Antibody (CSB-PA896740LA01HU)，的標記方式是Non-conjugated。對于GMPPB Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產(chǎn)品名稱	應用
HRP	CSB-PA896740LB01HU	GMPPB Antibody, HRP conjugated	ELISA
FITC	CSB-PA896740LC01HU	GMPPB Antibody, FITC conjugated
Biotin	CSB-PA896740LD01HU	GMPPB Antibody, Biotin conjugated	ELISA

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
應用范圍：

ELISA, IHC

推薦稀釋比：

Application	Recommended Dilution
IHC	1:20-1:200

Protocols：

ELISA Protocol
Immunohistochemistry (IHC) 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(chǎn)品評價

靶點詳情

功能：

Catalyzes the formation of GDP-mannose, an essential precursor of glycan moieties of glycoproteins and glycolipids.
基因功能參考文獻：
1. Late-onset limb-girdle muscular dystrophy caused by GMPPB mutations. PMID: 28478914
2. Study finds that the GMPPB mutation spectrum in Chinese patients may differ from that of European populations, with the mutation p.(Arg357His) most frequently found. These mutations may lead to abnormal folding of GMPPB leading to protein aggregates in the cytoplasm rather than an overall loss in protein expression. PMID: 28433477
3. Patients with GMPPB-CMS have phenotypic features aligned with CMS subtypes harbouring mutations within the early stages of the glycosylation pathway. Additional features shared with the dystroglycanopathies include myopathic features, raised Creatine Kinase levels and variable mild cognitive delay. PMID: 27147698
4. We observe that c.79G>C (p.D27H) is associated with a mild limb-girdle muscular dystrophy phenotype, whereas c.860G>A (p.R287Q) is associated with a relatively severe congenital muscular dystrophy typically involving brain development. PMID: 26310427
5. This study found mutations in GMPPB can lead to a wide spectrum of clinical features where deficit in neuromuscular transmission is the major component in a subset of cases. PMID: 26133662
6. The phenotypic spectrum of GMPPB mutations was expanded to include limb-girdle muscular dystrophies. PMID: 25681410
7. Work confirms a role for GMPPB defects in alpha-dystroglycanopathy, and suggests that glycosylation may play a role in the neuronal membrane channels or networks involved in the physiology of generalized epilepsy syndromes. PMID: 24780531
8. Individuals with GMPPB mutations have hypoglycosylated alpha-dystroglycan in muscle. These mutations cause congenital and limb-girdle muscular dystrophies. PMID: 23768512
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相關疾病：

Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A14 (MDDGA14); Muscular dystrophy-dystroglycanopathy congenital with mental retardation B14 (MDDGB14); Muscular dystrophy-dystroglycanopathy limb-girdle C14 (MDDGC14)
亞細胞定位：

Cytoplasm.
蛋白家族：

Transferase hexapeptide repeat family
數(shù)據(jù)庫鏈接：

HGNC: 22932

OMIM: 615320

KEGG: hsa:29925

UniGene: Hs.567488

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