TCTA Antibody, HRP conjugated

說明書

產品詳情

產品名稱：

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

P57738
基因名：

TCTA
別名：

T-cell leukemia translocation altered gene antibody; T-cell leukemia translocation-altered gene protein antibody; T-cell leukemia translocation-associated gene protein antibody; Tcta antibody; TCTA_HUMAN antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human T-cell leukemia translocation-altered gene protein (62-103AA)
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：

Antigen Affinity 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：

May be required for cellular fusion during osteoclastogenesis.
基因功能參考文獻：
1. TCTA protein has roles in lung cancer cell lines and human osteoclastogenesis [review] PMID: 22174563
2. It expressed in synovial tissues from patients with RA and inhibits human osteoclastogenesis. (review) PMID: 20046013
3. TCTA is a novel protein expressed in synovial tissues of rheumatoid arthritis that regulate human osteoclastogenesis. PMID: 19560569
相關疾病：

A chromosomal aberration involving TCTA is associated with T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(1;3)(p34;p21).
亞細胞定位：

Membrane; Multi-pass membrane protein.
蛋白家族：

TCTA family
組織特異性：

Ubiquitous. Highest level of expression in kidney. Present in monocytes, osteoclasts, macrophages, synoviocytes and synovial lining cells (at protein level).
數據庫鏈接：

HGNC: 11692

OMIM: 600690

KEGG: hsa:6988

STRING: 9606.ENSP00000273590

UniGene: Hs.517962

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