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SLC39A13 Rabbit pAb (bs-21283R)  
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產(chǎn)品編號(hào) bs-21283R
英文名稱 SLC39A13 Rabbit pAb
中文名稱 溶質(zhì)載體轉(zhuǎn)運(yùn)蛋白家族39成員A13抗體
別    名 FLJ25785; LIV-1 subfamily of ZIP zinc transporter 9; LZT-Hs9; S39AD_HUMAN; SLC39A13; solute carrier family 39(metal ion transporter), member 13; solute carrier family 39(zinc transporter), member 13; Solute carrier family 39 member 13; Zinc transporter ZI  
研究領(lǐng)域 細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  轉(zhuǎn)運(yùn)蛋白  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,Rat (predicted: Human)
產(chǎn)品應(yīng)用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 39 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC39A13: 1-100/371 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome.[provided by RefSeq, Mar 2010]

Function:
Acts as a zinc-influx transporter.

Subcellular Location:
Membrane.

DISEASE:
Defects in SLC39A13 are the cause of Ehlers-Danlos syndrome-like spondylocheirodysplasia (SCD-EDS) [MIM:612350]. SCD-EDS is a 'spondylocheiro dysplastic form of Ehlers-Danlos syndrome'. The syndrome consists of a generalized skeletal dysplasia involving mainly the spine (spondylo) and striking clinical abnormalities of the hands (cheiro) in addition to the EDS-like features. Clinical features included postnatal growth retardation, moderate short stature, protuberant eyes with bluish sclerae, hands with finely wrinkled palms, atrophy of the thenar muscles, and tapering fingers. Patients have thin, hyperelastic skin and hypermobile small joints consistent with an Ehlers-Danlos-like phenotype. Radiologic features included mild to moderate platyspondyly, mild to moderate osteopenia of the spine, small ileum, flat proximal femoral epiphyses, short, wide femoral necks, and broad metaphyses (elbows, knees, wrists, and interphalangeal joints).

Similarity:
Belongs to the ZIP transporter (TC 2.A.5) family.

SWISS:
Q96H72

Gene ID:
91252

Database links:

Entrez Gene: 101095193 Cat

Entrez Gene: 743682 Chimpanzee

Entrez Gene: 614946 Cow

Entrez Gene: 475981 Dog

Entrez Gene: 91252 Human

Entrez Gene: 68427 Mouse

Entrez Gene: 713420 Rhesus monkey

Omim: 608735 Human

SwissProt: A5D7H1 Cow

SwissProt: Q96H72 Human

SwissProt: Q8BZH0 Mouse

Unigene: 523664 Human

Unigene: 192375 Mouse



產(chǎn)品圖片
Sample: Lane 1: Mouse Skin tissue lysates Lane 2: Rat Skin tissue lysates Primary: Anti-SLC39A13 (bs-21283R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 39 kDa Observed band size: 42 kDa
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