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ELK Biotechnology ZAP-70 (phospho Tyr315) rabbit pAb
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ELK Biotechnology ZAP-70 (phospho Tyr315) rabbit pAb

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ZAP-70 (phospho Tyr315) rabbit polyclonal antibody로 T세포 발달 및 활성화 연구에 적합. WB, IHC, IF, ELISA 등 다양한 응용 가능. 인산화 Tyr315 부위 기반 면역원 사용. 사람 및 생쥐 반응성. -20°C에서 1년 보관 가능.

판매단위
pk
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ELK Biotechnology ES7531-100UL ZAP-70 (phospho Tyr315) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7531-50UL ZAP-70 (phospho Tyr315) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology ZAP-70 (phospho Tyr315) rabbit pAb

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ZAP-70 (phospho Tyr315) 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 Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human ZAP-70 around the phosphorylation site of Tyr315 (AA range: 281-330)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 60 kD
Gene ID (Human) 7535
Human Swiss-Prot No. P43403
Species Reactivity Human; Mouse
Cellular Localization Cytoplasm, Cell membrane; Peripheral membrane protein. In quiescent T-lymphocytes, cytoplasmic. Upon TCR activation, recruited to plasma membrane via CD247/CD3Z interaction. Colocalizes with RHOH in the immunological synapse. RHOH is required for proper localization to membrane and cytoskeleton fractions in thymocytes (By similarity).

Background

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

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