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ELK Biotechnology ZAP-70 (phospho Tyr319) rabbit pAb
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ELK Biotechnology ZAP-70 (phospho Tyr319) rabbit pAb

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ZAP-70 (phospho Tyr319) rabbit pAb는 인산화된 ZAP-70 단백질을 검출하는 폴리클로날 항체로, T세포 신호전달 연구에 적합합니다. WB, IHC, IF, ELISA에 사용 가능하며, 사람·마우스·랫에서 반응합니다. 고순도 IgG 형태로 -20°C에서 1년 보관 가능합니다.

판매단위
pk
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ELK Biotechnology ES7528-100UL ZAP-70 (phospho Tyr319) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7528-50UL ZAP-70 (phospho Tyr319) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology ZAP-70 (phospho Tyr319) rabbit pAb

제품명

ZAP-70 (phospho Tyr319) rabbit pAb

제품 정보

항목 내용
Alternative Names ZAP70; SRK; Tyrosine-protein kinase ZAP-70; 70 kDa zeta-chain associated protein; Syk-related tyrosine kinase
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000
IHC: 1/100–1/300
IF: 1/200–1/1000
ELISA: 1/20000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human ZAP-70 around the phosphorylation site of Tyr319 (AA range: 286–335)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 70 kDa
Gene ID (Human) 7535
Human Swiss-Prot No. P43403
Species Reactivity Human; Mouse; Rat
Cellular Localization Cytoplasm; Cell membrane; Peripheral membrane protein. In quiescent T-lymphocytes, it is cytoplasmic. Upon TCR activation, recruited to the plasma membrane via CD247/CD3Z interaction. Colocalizes with RHOH in the immunological synapse. RHOH is required for proper localization to the membrane and cytoskeleton in thymocytes (By similarity).

Background

This gene encodes an enzyme belonging to the protein tyrosine kinase family, which plays a key role in T-cell development and lymphocyte activation. The enzyme becomes phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation and functions in the initial step of TCR-mediated signal transduction together with Src family kinases Lck and Fyn. It is essential for thymocyte development, and mutations in this gene cause selective T-cell defects, leading to severe combined immunodeficiency characterized by the absence of CD8-positive T-cells. Two transcript variants encoding different isoforms have been identified (RefSeq, Jul 2008).

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