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ELK Biotechnology NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb
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ELK Biotechnology NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb

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NMDAε1/2 인산화 타이로신(Tyr1246/1252)을 인식하는 토끼 폴리클로날 항체. WB, IHC, IF, ELISA에 사용 가능. 인간 NMDAR2A/B 유래 합성 펩타이드로 면역화. 시냅스 및 수상돌기막 발현 연구에 적합. -20°C 보관.

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pk
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ELK Biotechnology ES5652-100UL NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5652-50UL NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb

제품명

NMDAε1/2 (phospho Tyr1246/1252) rabbit pAb

제품 정보

항목 내용
Alternative Names GRIN2A; NMDAR2A; Glutamate [NMDA] receptor subunit epsilon-1; N-methyl D-aspartate receptor subtype 2A; NMDAR2A; NR2A; hNR2A; GRIN2B; NMDAR2B; Glutamate [NMDA] receptor subunit epsilon-2; N-methyl D-aspartate receptor subtype 2B; NMDAR2B
Applications WB; IHC; IF; ELISA
Recommended Dilutions IHC: 1/100–1/300
IF: 1/200–1/1000
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human NMDAR2A/B around the phosphorylation site of Tyr1246/1252 (AA range: 1216–1265)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
GeneID (Human) 2903 / 2904
Human Swiss-Prot No. Q12879 / Q13224
Species Reactivity Human; Mouse; Rat
Cellular Localization Cell projection, dendritic spine; Cell membrane (multi-pass membrane protein); Cell junction, synapse; Postsynaptic cell membrane; Cytoplasmic vesicle membrane. Expression at dendrite cell membrane and synapses is regulated by SORCS2 and the retromer complex.

Background

This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without mental retardation. Alternative splicing results in multiple transcript variants. (RefSeq, May 2014)

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