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ERPINA6/Cortisol Binding Globulin Rabbit pAb (bs-14001R)  
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產品編號 bs-14001R
英文名稱 ERPINA6/Cortisol Binding Globulin Rabbit pAb
中文名稱 皮質醇結合球蛋白抗體
別    名 CBG; CBG_HUMAN; corticosteroid binding globulin; Corticosteroid-binding globulin; serine(or cysteine) proteinase inhibitor clade A(alpha 1 antiproteinase antitrypsin) member 6; serpin A6; serpin peptidase inhibitor clade A(alpha 1 antiproteinase antitryps  
研究領域 腫瘤  轉運蛋白  結合蛋白  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human (predicted: Mouse,Sheep,Cow)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 43 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Cortisol Binding Globulin: 121-220/405 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008]

Function:
Major transport protein for glucocorticoids and progestins in the blood of almost all vertebrate species.

Subcellular Location:
Secreted.

Tissue Specificity:
Plasma; synthesized in liver. Has also been identified in a number of glycocorticoid responsive cells.

Post-translational modifications:
N-glycosylated; binds 5 oligosaccharide chains.
Glycosylation in position Asn-260 is needed for steroid binding.

DISEASE:
Defects in SERPINA6 are a cause of corticosteroid-binding globulin deficiency (CBG deficiency) [MIM:611489]. CBG deficiency is an extremely rare hereditary disorder characterized by reduced corticosteroid-binding capacity with normal or low plasma corticosteroid-binding globulin concentration, and normal or low basal cortisol levels associated with hypo/hypertension and muscle fatigue.

Similarity:
Belongs to the serpin family.

SWISS:
P08185

Gene ID:
866

Database links:

Entrez Gene: 866 Human

Omim: 122500 Human

SwissProt: P08185 Human

Unigene: 532635 Human



產品圖片
Sample: HepG2(Human) Cell Lysate at 30 ug Primary: Anti- Cortisol Binding Globulin (bs-14001R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 43 kD Observed band size: 73 kD
Paraformaldehyde-fixed, paraffin embedded Human Liver; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with ERPINA6 Polyclonal Antibody, Unconjugated (bs-14001R) at 1:200 overnight at 4°C, followed by conjugation to the SP Kit (Rabbit, SP-0023) and DAB (C-0010) staining.
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