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SLC7A14 Antibody, Biotin conjugated

說明書

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) SLC7A14 Polyclonal antibody
Uniprot No.：

Q8TBB6
基因名：

SLC7A14
別名：

SLC7A14 antibody; KIAA1613 antibody; Probable cationic amino acid transporter antibody; Solute carrier family 7 member 14 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Probable cationic amino acid transporter protein (676-771AA)
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Biotin
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：

May be involved in arginine transport.
基因功能參考文獻(xiàn)：
1. The four SLC7A14 mutations detected herein were unlikely to be pathogenic in this Japanese cohort. The frequency and pathogenicity of SLC7A14 mutations may vary depending on ethnicity, and these mutations may be rare in Japanese patients. PMID: 27028480
2. Data suggests that cationic transporter SLC7A14 has an important role in retinal development and visual function. PMID: 24670872
3. A chimera carrying the functional domain of the orphan protein SLC7A14 in the backbone of SLC7A2 mediates trans-stimulated arginine transport. PMID: 22787143
相關(guān)疾病：

Retinitis pigmentosa 68 (RP68)
亞細(xì)胞定位：

Lysosome membrane; Multi-pass membrane protein. Note=Exhibits a punctated pattern in the cytoplasm, which partially ovelaps with lysosomes.
蛋白家族：

Amino acid-polyamine-organocation (APC) superfamily, Cationic amino acid transporter (CAT) (TC 2.A.3.3) family
組織特異性：

Expressed in skin fibroblasts.
數(shù)據(jù)庫鏈接：

HGNC: 29326

OMIM: 615720

KEGG: hsa:57709

STRING: 9606.ENSP00000231706

UniGene: Hs.596660

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