PEX10 Antibody, Biotin conjugated

說明書

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) PEX10 Polyclonal antibody
Uniprot No.：

O60683
基因名：

PEX10
別名：

AV128229 antibody; Gm142 antibody; MGC1998 antibody; NALD antibody; OTTHUMP00000001658 antibody; PBD6A antibody; PBD6B antibody; peroxin 10 antibody; Peroxin-10 antibody; Peroxisomal biogenesis factor 10 antibody; Peroxisome assembly protein 10 antibody; Peroxisome biogenesis factor 10 antibody; PEX10 antibody; PEX10_HUMAN antibody; RING finger protein 69 antibody; RNF69 antibody; RP23-298E4.1 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Peroxisome biogenesis factor 10 protein (63-157AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

Biotin
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA
Protocols：

ELISA Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

功能：

Somewhat implicated in the biogenesis of peroxisomes.
基因功能參考文獻：
1. This study demonstrated that two mutations in PEX10 were found in the three peroxisomal biogenesis disorders patients: c.827G>T (novel) causing the missense change p.Cys276Phe and c.932G>A causing the missense change p.Arg311Gln. PMID: 27230853
2. abnormal expression of PEX10 gene resulting from copy number variations of 1p36 region may be associated with the epilepsy phenotype PMID: 25636090
3. child and an adult of normal intelligence with progressive ataxia, axonal motor neuropathy, decreased vibration sense and cerebellar atrophy; 2 mutations in PEX10 found in child, c.992G>A and c.764_765insA, and in the adult, c.2T>C and c.790C>T PMID: 20695019
4. Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. PMID: 14713216
5. the relative fraction of disease-causing alleles that occur in the coding and splice junction sequences of PEX10 gene. PMID: 19105186
顯示更多

收起更多
相關疾病：

Peroxisome biogenesis disorder complementation group 7 (PBD-CG7); Peroxisome biogenesis disorder 6A (PBD6A); Peroxisome biogenesis disorder 6B (PBD6B)
亞細胞定位：

Peroxisome membrane; Peripheral membrane protein.
蛋白家族：

Pex2/pex10/pex12 family
數據庫鏈接：

HGNC: 8851

OMIM: 602859

KEGG: hsa:5192

UniGene: Hs.732228

YWHAB Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF, FC

Species Reactivity: Human, Mouse, Rat
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
XRCC5 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF

Species Reactivity: Human
XPNPEP1 Recombinant Monoclonal Antibody

Applications: ELISA, IHC, FC

Species Reactivity: Human
XDH Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WT1 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WFDC2 Recombinant Monoclonal Antibody

Applications: ELISA, WB, FC

Species Reactivity: Human
WDR5 Recombinant Monoclonal Antibody

Applications: ELISA, IHC, FC

Species Reactivity: Human