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CACNA1F Rabbit mAb

商品貨號： PRM8201

適應(yīng) 性： Human

￥800元

規(guī)格：

50ul

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MSDS

說明書

商品描述

發(fā)貨日期：現(xiàn)貨
靶點-Target： CAC1F
反應(yīng)性-Reactivity： Human
應(yīng)用-Applications： WB,Flow Cyt
MW(Observed)： 217kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-5000;FC 1:100-300
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0769R
特異性： Endogenous
基因名稱： CACNA1F;CACNAF1
蛋白名稱： Voltage-dependent L-type calcium channel subunit alpha-1F;Voltage-gated calcium channel subunit alpha Cav1.4;
別名： CACNA1F;CACNAF1;Voltage-dependent L-type calcium channel subunit alpha-1F ;Voltage-gated calcium channel subunit alpha Cav1.4;
Organism-1： Human
基因ID-1： 778
SwissProt-1： O60840
Organism-2： Mouse
SwissProt-2： Q9JIS7
背景： calcium voltage-gated channel subunit alpha1 F(CACNA1F) Homo sapiens This gene encodes a multipass transmembrane protein that functions as an alpha-1 subunit of the voltage-dependent calcium channel, which mediates the influx of calcium ions into the cell. The encoded protein forms a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Mutations in this gene can cause X-linked eye disorders, including congenital stationary night blindness type 2A, cone-rod dystropy, and Aland Island eye disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2013],
細胞定位： Membrane; Multi-pass membrane protein.

CACNA1F Rabbit mAb

Catalog No PRM8201

Product information

發(fā)貨日期：現(xiàn)貨
靶點-Target： CAC1F
反應(yīng)性-Reactivity： Human
應(yīng)用-Applications： WB,Flow Cyt
MW(Observed)： 217kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-5000;FC 1:100-300
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0769R
特異性： Endogenous
基因名稱： CACNA1F;CACNAF1
蛋白名稱： Voltage-dependent L-type calcium channel subunit alpha-1F;Voltage-gated calcium channel subunit alpha Cav1.4;
別名： CACNA1F;CACNAF1;Voltage-dependent L-type calcium channel subunit alpha-1F ;Voltage-gated calcium channel subunit alpha Cav1.4;
Organism-1： Human
基因ID-1： 778
SwissProt-1： O60840
Organism-2： Mouse
SwissProt-2： Q9JIS7
背景： calcium voltage-gated channel subunit alpha1 F(CACNA1F) Homo sapiens This gene encodes a multipass transmembrane protein that functions as an alpha-1 subunit of the voltage-dependent calcium channel, which mediates the influx of calcium ions into the cell. The encoded protein forms a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Mutations in this gene can cause X-linked eye disorders, including congenital stationary night blindness type 2A, cone-rod dystropy, and Aland Island eye disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2013],
細胞定位： Membrane; Multi-pass membrane protein.

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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