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ELK Biotechnology ZAP-70 (phospho Tyr292) rabbit pAb
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ELK Biotechnology ZAP-70 (phospho Tyr292) rabbit pAb

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인간 및 마우스에 반응하는 ZAP-70 (phospho Tyr292) rabbit polyclonal antibody로, T세포 신호전달 관련 단백질 검출에 적합. WB 및 ELISA에 사용 가능하며, 고순도 IgG 형태로 안정적 저장 가능. TCR 활성화 및 면역학 연구에 유용.

판매단위
pk
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ELK Biotechnology ES7530-100UL ZAP-70 (phospho Tyr292) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7530-50UL ZAP-70 (phospho Tyr292) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology ZAP-70 (phospho Tyr292) rabbit pAb

제품명

ZAP-70 (phospho Tyr292) rabbit pAb

기본 정보

항목 내용
Alternative Names ZAP70; SRK; Tyrosine-protein kinase ZAP-70; 70 kDa zeta-chain associated protein; Syk-related tyrosine kinase
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human ZAP-70 around the phosphorylation site of Tyr292 (AA range: 258–307)
Species Reactivity Human; Mouse
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 70 kDa
GeneID (Human) 7535
Human Swiss-Prot No P43403
Cellular Localization Cytoplasm; Cell membrane; Peripheral membrane protein. In quiescent T-lymphocytes, it is cytoplasmic. Upon TCR activation, it is recruited at the plasma membrane by interacting with CD247/CD3Z. Colocalizes together with RHOH in the immunological synapse. RHOH is required for its proper localization to the cell membrane and cytoskeleton fractions in thymocytes (By similarity).
Storage -20°C / 1 year
Host Rabbit

Background

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

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