ABCA12 Antibody, Biotin conjugated

說明書

中文名稱：

ABCA12兔多克隆抗體, Biotin偶聯
貨號：

CSB-PA774804LD01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) ABCA12 Polyclonal antibody
Uniprot No.：

Q86UK0
基因名：

ABCA12
別名：

ABC transporter A family member 12 antibody; ABC transporter ABCA.12 antibody; ABC12 antibody; ABCA12 antibody; ABCAC_HUMAN antibody; AtABCA12 antibody; ATH16 antibody; ATP binding cassette 12 antibody; ATP binding cassette sub family A (ABC1) member 12 antibody; ATP binding cassette sub family A member 12 antibody; ATP binding cassette transporter 12 antibody; ATP-binding cassette 12 antibody; ATP-binding cassette sub-family A member 12 antibody; ATP-binding cassette transporter 12 antibody; Ichthyosis congenita II lamellar ichthyosis B antibody; ICR2B antibody; LI2 antibody; Putative ABC2 homolog 16 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human ATP-binding cassette sub-family A member 12 protein (45-158AA)
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.

產品評價

靶點詳情

功能：

Transports lipids such as glucosylceramides from the outer to the inner leaflet of lamellar granules (LGs) membrane, whereby the lipids are finally transported to the keratinocyte periphery via the trans-Golgi network and LGs and released to the apical surface of the granular keratinocytes to form lipid lamellae in the stratum corneum of the epidermis, which is essential for skin barrier function. In the meantime, participates in the transport of the lamellar granules-associated proteolytic enzymes, in turn regulates desquamation and keratinocyte differentiation. Furthermore, is essential for the regulation of cellular cholesterol homeostasis by regulating ABCA1-dependent cholesterol efflux from macrophages through interaction with NR1H2 and ABCA1. Plays pleiotropic roles in regulating glucose stimulated insulin secretion from beta cells, regulating the morphology and fusion of insulin granules, lipid raft abundance and the actin cytoskeleton. Also involved in lung surfactant biogenesis.
基因功能參考文獻：
1. A novel heterozygous missense mutation was identified in ATP-binding cassette sub-family A member 12 (ABCA12) within a family afflicted with keratosis pilaris. In addition, upregulated ABCA12 expression levels in the sebaceous glands of patients with nevus comedonicus were investigated. PMID: 30066947
2. the present study has identified a novel homozygous deleterious intronic variant, which is associated with a severe phenotype of HI. PMID: 29377090
3. two missense ABCA12 mutations were uncovered in both of the affected brothers. PMID: 28236338
4. we identified three novel mutations and one reported mutation in the TGM1 and ABCA12 genes, respectively, in affected siblings of five Saudi unrelated families PMID: 27061915
5. Genes ABCC7, A3, A8, A12, and C8 prevailed among the most upregulated or downregulated ones. In conclusion, the results supported our theory about general adenosine triphosphate-binding cassette gene expression profiles and their importance for cancer on clinical as well as research levels. PMID: 28468577
6. Autosomal recessive inheritance of mutations in the ATP-binding cassette, subfamily A, member 12 (ABCA12, OMIM*607800, chromosome 2q35) gene was found to be responsible for the disease. PMID: 25563821
7. Identification of the key promoter element of ABCA12 in this study may provide relevant information for genetic diagnosis of recessive congenital ichthyosis. PMID: 25338618
8. Ssnger sequencing of the parents of neonates deceased patients with Harlequin ichthyosis identified novel mutations in ABCA12 gene. PMID: 25479012
9. ABCA12 mutations result in defective lipid transport via lamellar granules in the keratinocytes, leading to ichthyosis phenotypes from malformation of the stratum corneum lipid barrier. PMID: 23954554
10. Report a consanguineous family of Arab Muslim origin with several members displaying a severe form of congenital ichthyosiform erythroderma. Identified a region of homozygosity shared by all patients on 2q34, in a region harbouring the ABCA12 gene. PMID: 23528209
11. We show that homozygosity for a novel c.4676G>T transition in the ABCA12 gene, resulting in a p.G1559V substitution, causes non-bullous congenital ichthyosiform erythroderms in 5 members of an extended family. PMID: 22257947
12. The authors report on a 2282del4 mutation that may be associated with ichthyosis vulgaris in a Pakistani population. PMID: 21712002
13. The researchers report on another fatal case of Harlequin ichthyosis that may be associated with mutations of the ABCA12 gene PMID: 21798141
14. AKT signaling helps ABCA12 deficient keratinocytes survive during the keratinization process. PMID: 21633372
15. Mutation analysis revealed that 52% of the survivors of harlequin ichthyosis had compound heterozygous mutations of ABCA12, whereas all deaths were associated with homozygous mutations of ABCA12. PMID: 21339420
16. loss of ABCA12 function leads to a defective lipid barrier in the stratum corneum, resulting in an ichthyotic phenotype (Review) PMID: 20672373
17. Our results clearly demonstrate that ABCA12 deficiency impairs glucosylceramide accumulation in lamellar bodies, thereby strongly indicating that ABCA12 transports glucosylceramide to the inner leaflet of lamellar bodies. PMID: 20869849
18. Cloning, characterization and chromosome mapping of ABCA12. PMID: 12697999
19. Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. PMID: 12915478
20. Sequencing of the ABCA12 gene, which maps within the minimal region defined by homozygosity mapping, revealed disease-associated mutations, including large intragenic deletions and frameshift deletions in 11 of the 12 screened individuals with HI. PMID: 15756637
21. 5 distinct ABCA12 mutations, either in a compound heterozygous or homozygous state, in patients from 4 harlequin ichthyosis families PMID: 16007253
22. These mutation data establish ABCA12 as the major harlequin ichthyosis gene. PMID: 16902423
23. study identified two novel ABCA12 mutations in two unrelated non-bullous congenital ichthyosiform erythroderma patients; both patients presented with multiple skin malignancies including malignant melanoma PMID: 17508018
24. Our findings demonstrate that ABCA12 is highly expressed in fetal skin and suggest that ABCA12 may play an essential role under both the wet and dry conditions. PMID: 17591952
25. PPAR and LXR activators regulate ABCA12 expression in human keratinocytes. PMID: 17611579
26. ABCA12 plays an important role in lipid transport from the Golgi apparatus to lamellar granules in human granular layer keratinocytes. PMID: 17927575
27. mutation analysis of twelve families demonstrated novel and recurring ABCA12 mutations PMID: 17986308
28. ABCA12 is reduced in harlequin ichrhyosis and thus is a key molecule in regulating keratinocyte differentiation and transporting specific proteases associated with desquamation. PMID: 19179616
29. ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma. PMID: 19262603
30. ceramide, an important lipid component of epidermis, up-regulates ABCA12 expression via the PPARdelta-mediated signaling pathway, providing a substrate-driven, feed-forward mechanism for regulating this key lipid transporter PMID: 19429679
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相關疾病：

Ichthyosis, congenital, autosomal recessive 4A (ARCI4A); Ichthyosis, congenital, autosomal recessive 4B (ARCI4B)
亞細胞定位：

Cytoplasmic vesicle, secretory vesicle membrane; Multi-pass membrane protein. Golgi apparatus membrane.
蛋白家族：

ABC transporter superfamily, ABCA family
組織特異性：

Mainly expressed in the stomach, placenta, testis and fetal brain. Expressed in the upper epidermal layers, mainly the granular layers, of skin. Expressed throughout the normal interfollicular epidermis with prominent expression in the stratum granulosum.
數據庫鏈接：

HGNC: 14637

OMIM: 242500

KEGG: hsa:26154

STRING: 9606.ENSP00000272895

UniGene: Hs.134585

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