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SEMA4A Polyclonal Antibody

商品貨號(hào)： PLA018061

適應(yīng) 性： 人,小鼠,大鼠,猴

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說(shuō)明書(shū)

商品描述

基因名稱： SEMA4A
蛋白名稱： Semaphorin-4A
Human_gene_id： 64218
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=64218
Human_swiss_prot_no： Q9H3S1
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9H3S1/entry
Mouse_gene_id： 20351
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20351
Mouse_swiss_prot_no： Q62178
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q62178
特異性： SEMA4A Polyclonal Antibody detects endogenous levels of SEMA4A protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:20000. Not yet tested in other applications.
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
其他名稱： SEMA4A; SEMAB; SEMB; Semaphorin-4A; Semaphorin-B; Sema B
實(shí)測(cè)條帶： 84kD
信號(hào)通路： Axon guidance;
功能： disease:Defects in SEMA4A are the cause of cone-rod dystrophy type 10 (CORD10) [MIM:610283]. CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa.,disease:Defects in SEMA4A are the cause of retinitis pigmentosa type 35 (RP35) [MIM:610282]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.,function:Inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons.,similarity:Belongs to the semaphorin family.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 1 PSI domain.,similarity:Contains 1 Sema domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane ; Single-pass type I membrane protein .
組織表達(dá)： Colon,Mammary gland,Placenta,Salivary gland,Tongue,
tag： hot
科研貨號(hào)： PLA018061

SEMA4A Polyclonal Antibody

Catalog No PLA018061

Product information

基因名稱： SEMA4A
蛋白名稱： Semaphorin-4A
Human_gene_id： 64218
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=64218
Human_swiss_prot_no： Q9H3S1
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9H3S1/entry
Mouse_gene_id： 20351
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20351
Mouse_swiss_prot_no： Q62178
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q62178
特異性： SEMA4A Polyclonal Antibody detects endogenous levels of SEMA4A protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:20000. Not yet tested in other applications.
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
其他名稱： SEMA4A; SEMAB; SEMB; Semaphorin-4A; Semaphorin-B; Sema B
實(shí)測(cè)條帶： 84kD
信號(hào)通路： Axon guidance;
功能： disease:Defects in SEMA4A are the cause of cone-rod dystrophy type 10 (CORD10) [MIM:610283]. CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa.,disease:Defects in SEMA4A are the cause of retinitis pigmentosa type 35 (RP35) [MIM:610282]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.,function:Inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons.,similarity:Belongs to the semaphorin family.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 1 PSI domain.,similarity:Contains 1 Sema domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane ; Single-pass type I membrane protein .
組織表達(dá)： Colon,Mammary gland,Placenta,Salivary gland,Tongue,
tag： hot
科研貨號(hào)： PLA018061

Hunan UPT Biotechnology Co.,Ltd

Website：www.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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