SYNC Antibody

產品詳情

產品名稱：

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

Q9H7C4
基因名：

SYNC
別名：

1110057H03Rik antibody; Intermediate filament protein syncoilin antibody; MGC124230 antibody; MGC149625 antibody; MGC149626 antibody; RP23-391E6.2 antibody; SNIP4 antibody; SYNC antibody; SYNC1 antibody; SYNCI_HUMAN antibody; Syncoilin antibody; Syncoilin intermediate filament 1 antibody; Syncoilin-1 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Syncoilin protein (332-482AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，SYNC Antibody (CSB-PA862034LA01HU)，的標記方式是Non-conjugated。對于SYNC Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產品名稱	應用
HRP	CSB-PA862034LB01HU	SYNC Antibody, HRP conjugated	ELISA
FITC	CSB-PA862034LC01HU	SYNC Antibody, FITC conjugated
Biotin	CSB-PA862034LD01HU	SYNC 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.

功能：

Atypical type III intermediate filament (IF) protein that may play a supportive role in the efficient coupling of mechanical stress between the myofibril and fiber exterior. May facilitate lateral force transmission during skeletal muscle contraction. Does not form homofilaments nor heterofilaments with other IF proteins.
基因功能參考文獻：
1. Syncoilin modulates peripherin filament network formation. PMID: 20587592
2. The differences in human syncoilin and beta-synemin mRNA ratios between Duchenne muscular dystrophy and normal muscles were not statistically significant PMID: 20199207
3. the result of this study raise the possibility that mutations in the gene encoding for syncoilin may underlie some forms of muscle disease. PMID: 16124004
亞細胞定位：

Cytoplasm, perinuclear region.
蛋白家族：

Intermediate filament family
數據庫鏈接：

HGNC: 28897

OMIM: 611750

KEGG: hsa:81493

STRING: 9606.ENSP00000386439

UniGene: Hs.712631

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