PRSS12 Antibody

中文名稱：

PRSS12兔多克隆抗體
貨號：

CSB-PA018812LA01HU
規(guī)格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA018812LA01HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human lung tissue using CSB-PA018812LA01HU at dilution of 1:100
其他：

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) PRSS12 Polyclonal antibody
Uniprot No.：

P56730
基因名：

PRSS12
別名：

BSSP 3 antibody; BSSP3 antibody; Leydin antibody; MGC12722 antibody; Motopsin antibody; MRT1 antibody; NETR_HUMAN antibody; Neurotrypsin antibody; protease; serine; 12 (neurotrypsin; motopsin) antibody; Prss12 antibody; Serine protease 12 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Neurotrypsin protein (631-874AA)
免疫原種屬：

Homo sapiens (Human)

標(biāo)記方式：

Non-conjugated

本頁面中的產(chǎn)品，PRSS12 Antibody (CSB-PA018812LA01HU)，的標(biāo)記方式是Non-conjugated。對于PRSS12 Antibody，我們還提供其他標(biāo)記。見下表：

標(biāo)記方式	貨號	產(chǎn)品名稱	應(yīng)用
HRP	CSB-PA018812LB01HU	PRSS12 Antibody, HRP conjugated	ELISA
FITC	CSB-PA018812LC01HU	PRSS12 Antibody, FITC conjugated
Biotin	CSB-PA018812LD01HU	PRSS12 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(yīng)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.

功能：

Plays a role in neuronal plasticity and the proteolytic action may subserve structural reorganizations associated with learning and memory operations.
基因功能參考文獻：
1. 4-base pair deletion in the neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation; findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function PMID: 12459588
相關(guān)疾病：

Mental retardation, autosomal recessive 1 (MRT1)
亞細(xì)胞定位：

Secreted.
蛋白家族：

Peptidase S1 family
組織特異性：

Brain and Leydig cells of the testis.
數(shù)據(jù)庫鏈接：

HGNC: 9477

OMIM: 249500

KEGG: hsa:8492

STRING: 9606.ENSP00000296498

UniGene: Hs.445857

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