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Rabbit Anti-C22orf32 antibody
多克隆  |   SKU:bs-22826R

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货号:bs-3351R
¥1280
订购号:bs-22826R
¥1138.00-2900.00
货期:现货
Rabbit Anti-C22orf32 antibody
反应物种(预测)

Human,Pig,Cow,Horse,Rabbit,Sheep

产品应用(已验证)

IHC

推荐稀释比例

IHC-P=1:100-500,

研究领域

细胞生物,免疫学,线抗体,

标签

Array

  • Paraformaldehyde-fixed, paraffin embedded (rat pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (C22orf32) Polyclonal Antibody, Unconjugated (bs-22826R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
  • Paraformaldehyde-fixed, paraffin embedded (mouse pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (C22orf32) Polyclonal Antibody, Unconjugated (bs-22826R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

产品信息

RRID:RRID
产品名称:Rabbit Anti-C22orf32 antibody
别名: Chromosome 22 open reading frame 32; EMRE_HUMAN; DDDD; dJ186O1.1; mitochondrial; UPF0466 protein C22orf32.
中文名称:22号染色体开放阅读框32抗体
英文名称:Rabbit Anti-C22orf32 antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞膜
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

免疫原信息

免 疫 原:KLH conjugated synthetic peptide derived from human C22orf32
抗原表位:41-107/107
SWISS:Q9H4I9
Gene ID :91689
Human Gene ID:91689

产品介绍

Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf32 gene product has been provisionally designated C22orf32 pending further characterization
Subcellular Location:Mitochondrion (Potential). Membrane; Single-pass membrane protein (Potential).
Similarity:Belongs to the UPF0466 family.
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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