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SLC6A8 Polyclonal Antibody

商品貨號： PLA018140

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： SLC6A8
蛋白名稱： Sodium- and chloride-dependent creatine transporter 1
Human_gene_id： 6535
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6535
Human_swiss_prot_no： P48029
Human_swiss_link： http://www.uniprot.org/uniprotkb/P48029/entry
Mouse_gene_id： 102857
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=102857
Mouse_swiss_prot_no： Q8VBW1
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8VBW1
Rat_gene_id： 50690
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50690
Rat_swiss_prot_no： P28570
Rat_swiss_link： http://www.uniprot.org/uniprot/P28570
特異性： SLC6A8 Polyclonal Antibody detects endogenous levels of SLC6A8 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： SLC6A8; Sodium- and chloride-dependent creatine transporter 1; CT1; Creatine transporter 1; Solute carrier family 6 member 8
實測條帶： 70kD
功能： disease:Defects in SLC6A8 are the cause of X-linked creatine deficiency syndrome [MIM:300352]. X-linked creatine deficiency syndrome causes developmental delay, hypotonia, mental retardation, seizures, short stature and midface hypoplasia.,function:Required for the uptake of creatine in muscles and brain.,similarity:Belongs to the sodium:neurotransmitter symporter (SNF) family.,tissue specificity:Predominantly expressed in skeletal muscle and kidney. Also found in brain, heart, colon, testis and prostate.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Membrane; Multi-pass membrane protein.
組織表達(dá)： Predominantly expressed in skeletal muscle and kidney. Also found in brain, heart, colon, testis and prostate.
科研貨號： PLA018140

SLC6A8 Polyclonal Antibody

Catalog No PLA018140

Product information

基因名稱： SLC6A8
蛋白名稱： Sodium- and chloride-dependent creatine transporter 1
Human_gene_id： 6535
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6535
Human_swiss_prot_no： P48029
Human_swiss_link： http://www.uniprot.org/uniprotkb/P48029/entry
Mouse_gene_id： 102857
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=102857
Mouse_swiss_prot_no： Q8VBW1
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8VBW1
Rat_gene_id： 50690
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50690
Rat_swiss_prot_no： P28570
Rat_swiss_link： http://www.uniprot.org/uniprot/P28570
特異性： SLC6A8 Polyclonal Antibody detects endogenous levels of SLC6A8 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： SLC6A8; Sodium- and chloride-dependent creatine transporter 1; CT1; Creatine transporter 1; Solute carrier family 6 member 8
實測條帶： 70kD
功能： disease:Defects in SLC6A8 are the cause of X-linked creatine deficiency syndrome [MIM:300352]. X-linked creatine deficiency syndrome causes developmental delay, hypotonia, mental retardation, seizures, short stature and midface hypoplasia.,function:Required for the uptake of creatine in muscles and brain.,similarity:Belongs to the sodium:neurotransmitter symporter (SNF) family.,tissue specificity:Predominantly expressed in skeletal muscle and kidney. Also found in brain, heart, colon, testis and prostate.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Membrane; Multi-pass membrane protein.
組織表達(dá)： Predominantly expressed in skeletal muscle and kidney. Also found in brain, heart, colon, testis and prostate.
科研貨號： PLA018140

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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