PIH1D3 Antibody, HRP conjugated

說明書

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) PIH1D3 Polyclonal antibody
Uniprot No.：

Q9NQM4
基因名：

PIH1D3
別名：

PIH1D3 antibody; CXorf41 antibody; Protein PIH1D3 antibody; PIH1 domain-containing protein 3 antibody; Sarcoma antigen NY-SAR-97 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Protein PIH1D3 protein (1-214AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

HRP
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
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：

Plays a role in cytoplasmic pre-assembly of axonemal dynein.
基因功能參考文獻：
1. Study propose that PIH1D3 is part of a complementary conserved R2TP-like HSP90 co-chaperone complex, the loss of which affects assembly of a subset of inner arm dyneins. PMID: 28176794
2. Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects PMID: 28041644
相關(guān)疾?。?/div>
Ciliary dyskinesia, primary, 36, X-linked (CILD36)
亞細胞定位：

Cytoplasm. Golgi apparatus, trans-Golgi network.
蛋白家族：

PIH1 family
組織特異性：

Expressed in testis, small intestine, prostate, adrenal gland, spleen, lung, bladder, breast and ovary. Expressed in ciliated epithelial cells.
數(shù)據(jù)庫鏈接：

HGNC: 28570

OMIM: 300933

KEGG: hsa:139212

STRING: 9606.ENSP00000337757

UniGene: Hs.128836