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重组人X染色体开放阅读框21蛋白
产品名称:
重组人X染色体开放阅读框21蛋白
英文名称:
Recombinant human TASL protein, N-His
产品类别:
蛋白多肽
产品编号:
bs-42236P
保存条件:
Stored at -70℃ or -20℃. Avoid repeated freeze/thaw
[价格]
规格 价格 库存
100ug ¥ 2980.00 10
500ug ¥ 9500.00 10

产品详情

产品编号bs-42236P
英文名称Recombinant human TASL protein, N-His
中文名称重组人X染色体开放阅读框21蛋白
别????名TASL; TLR adapter interacting with SLC15A4 on the lysosome; Chromosome X open reading frame 21; FLJ11577; Hypothetical protein LOC80231; Uncharacterized protein CXorf21; CX021_HUMAN.??
性????状Lyophilized or Liquid
浓????度>1mg/ml
物????种Human
序????列1-301/301
纯????度>90% as determined by SDS-PAGE
纯化方法AC
内毒素Not analyzed
表达系统E.coli
标签N-His
缓?冲?液20mM Tris-Hcl (pH=8.0) with 8M Urea
保存条件Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

SWISS:
Q9HAI6

Gene ID:
80231

产品图片
The purity of the protein is greater than 85% as determined by reducing SDS-PAGE.

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