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SRPX2 抗体 (AA 166-465)
SRPX2
适用: 人
WB
宿主: 兔
Polyclonal
unconjugated
SRPX2抗体详情
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抗原
See all SRPX2 抗体
SRPX2
(Sushi-Repeat Containing Protein, X-Linked 2 (SRPX2))
抗原表位
All epitopes for SRPX2 抗体
AA 166-465
适用
All reactivities for SRPX2 抗体
人
宿主
All hosts for SRPX2 抗体
兔
克隆类型
All clonalities for SRPX2 抗体
多克隆
标记
All conjugates for SRPX2 抗体
This SRPX2 antibody is un-conjugated
应用范围
All applications for SRPX2 抗体
Western Blotting (WB)
原理
SRPX2 Rabbit pAb
序列
DGRWSGGEPV CVDIDPPKIR CPHSREKMAE PEKLTARVYW DPPLVKDSAD GTITRVTLRG PEPGSHFPEG EHVIRYTAYD RAYNRASCKF IVKVQVRRCP TLKPPQHGYL TCTSAGDNYG ATCEYHCDGG YDRQGTPSRV CQSSRQWSGS PPICAPMKIN VNVNSAAGLL DQFYEKQRLL IISAPDPSNR YYKMQISMLQ QSTCGLDLRH VTIIELVGQP PQEVGRIREQ QLSANIIEEL RQFQRLTRSY FNMVLIDKQG IDRDRYMEPV TPEEIFTFID DYLLSNQELT QRREQRDICE
交叉反应
小鼠
产品特性
Polyclonal Antibodies
纯化方法
Affinity purification
免疫原
Recombinant fusion protein containing a sequence corresponding to amino acids 166-465 of human SRPX2 (NP_055282.1).
亚型
IgG
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Alternatives
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anti-Sushi-Repeat Containing Protein, X-Linked 2 (SRPX2) (Internal Region) antibody
SRPX2
适用: 小鼠, 人, 猴, Bat, 兔, Cow, 犬, 豚鼠, 马, Pig
IHC, IHC (p)
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
WB,1:200 - 1:2000
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
SRPX2目标详情
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抗原
SRPX2
(Sushi-Repeat Containing Protein, X-Linked 2 (SRPX2))
别名
SRPX2 (SRPX2 产品 )
别名
BPP antibody, CBPS antibody, PMGX antibody, RESDX antibody, SRPUL antibody, 1110039C07Rik antibody, SRP antibody, RGD1562444 antibody, sushi repeat containing protein, X-linked 2 antibody, sushi-repeat-containing protein, X-linked 2 antibody, SRPX2 antibody, Srpx2 antibody
背景
This gene encodes a secreted protein that contains three sushi repeat motifs. The encoded protein may play a role in the development of speech and language centers in the brain. This protein may also be involved in angiogenesis. Mutations in this gene are the cause of bilateral perisylvian polymicrogyria, rolandic epilepsy, speech dyspraxia and mental retardation.,SRPX2,BPP,CBPS,PMGX,RESDX,SRPUL,Neuroscience,SRPX2
分子量
52kDa
基因ID
27286
UniProt
O60687
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