TMEM87B Antibody

中文名稱：

TMEM87B兔多克隆抗體
貨號：

CSB-PA023891LA01HU
規格：

￥440
圖片：
IHC image of CSB-PA023891LA01HU diluted at 1:400 and staining in paraffin-embedded human prostate tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
其他：

產品詳情

標記方式：

Non-conjugated

本頁面中的產品，TMEM87B Antibody (CSB-PA023891LA01HU)，的標記方式是Non-conjugated。對于TMEM87B 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-PA023891LB01HU	TMEM87B Antibody, HRP conjugated	ELISA
FITC	CSB-PA023891LC01HU	TMEM87B Antibody, FITC conjugated
Biotin	CSB-PA023891LD01HU	TMEM87B 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, IHC

推薦稀釋比：

Application	Recommended Dilution
IHC	1:200-1:500

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.

功能：

May be involved in retrograde transport from endosomes to the trans-Golgi network (TGN).
基因功能參考文獻：
1. Heterozygous loss of FBLN7 and TMEM87B account for some of the clinical features, including cardiac defects and craniofacial abnormalities associated with 2q13 deletion syndrome. PMID: 24694933
相關疾病：

TMEM87B mutations may be involved in restrictive cardiomyopathy (RCM), a rare non-ischemic myocardial disease. RCM is characterized by restrictive ventricular-filling physiology in the presence of normal or reduced diastolic and/or systolic volumes (of 1 or both ventricles), biatrial enlargement, and normal ventricular wall thickness.
亞細胞定位：

Golgi apparatus membrane; Multi-pass membrane protein.
蛋白家族：

LU7TM family, TMEM87 subfamily
數據庫鏈接：

HGNC: 25913

OMIM: 617203

KEGG: hsa:84910

STRING: 9606.ENSP00000283206

UniGene: Hs.656298

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