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Rabbit Anti-SNX32/Gold Conjugated antibody (bs-16118R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-16118R-Gold
英文名稱1 Rabbit Anti-SNX32/Gold Conjugated antibody
中文名稱 膠體金標記的選擇連接蛋白32抗體
別    名 DKFZp761P1320; FLJ30934; MGC42112; MGC57276; SNX32; SNX32_HUMAN; SNX6B; Sortin nexin 32; Sortin nexin 6B; Sorting nexin-32; Sorting nexin-6B.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 細胞生物  免疫學  信號轉導  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Horse, )
產(chǎn)品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 46kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SNX32
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
SNX32 is a 403 amino acid protein that contains one PX (phox homology) domain and belongs to the sorting nexin family. Existing as two alternatively spliced isoforms, SNX32 may be involved in several stages of intracellular trafficking. The gene that encodes SNX32 consists of approximately 23,256 bases and maps to human chromosome 11q13.1. Housing over 1,400 genes and comprising nearly 4% of the human genome, chromosome 11 is considered a gene and disease association-dense chromosome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that map to chromosome 11. In addition, the blood disorders Sickle cell anemia and thalassemia are caused by mutations in the HBB gene, which is located on chromosome 11.

Function:
May be involved in several stages of intracellular trafficking.

Similarity:
Belongs to the sorting nexin family.
Contains 1 PX (phox homology) domain.

Database links:

Entrez Gene: 254122 Human

SwissProt: Q86XE0 Human

Unigene: 591950 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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