Anti-COL4A5 Antibody (CAB16360)
- SKU:
- CAB16360
- Product type:
- Antibody
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
| 抗体名: | Anti-COL4A5 Antibody |
| 抗体コード: | CAB16360 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | IHC |
| 反応性: | Rat |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1462-1691 of human COL4A5 (NP_203699.1). |
| 申し込み: | IHC |
| 推奨希釈: | IHC 1:50 - 1:200 |
| 反応性: | Rat |
| ポジティブサンプル: |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1462-1691 of human COL4A5 (NP_203699.1). |
| 精製方法: | Affinity purification |
| ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | SSVA HGFL ITRH SQTT DAPQ CPQG TLQV YEGF SLLY VQGN KRAH GQDL GTAG SCLR RFST MPFM FCNI NNVC NFAS RNDY SYWL STPE PMPM SMQP LKGQ SIQP FISR CAVC EAPA VVIA VHSQ TIQI PHCP QGWD SLWI GYSF MMHT SAGA EGSG QALA SPGS CLEE FRSA PFIE CHGR GTCN YYAN SYSF WLAT VDVS DMFS KPQS ETLK AGDL RTRI SRCQ VCMK RT |
| 遺伝子ID: | 1287 |
| Uniprot: | P29400 |
| セルラーロケーション: | Secreted, basement membrane, extracellular matrix, extracellular space |
| 計算された分子量: | 161kDa |
| 観察された分子量: |
| 同義語: | COL4A5, ASLN, ATS, CA54 |
| バックグラウンド: | This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. |
| UniProt Protein Function: | COL4A5: Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen. Defects in COL4A5 are the cause of Alport syndrome X- linked (APSX). APSX is characterized by progressive glomerulonephritis, renal failure, sensorineural deafness, specific eye abnormalities (lenticonous and macular flecks), and glomerular basement membrane defects. The disorder shows considerable heterogeneity in that families differ in the age of end-stage renal disease and the occurrence of deafness. Deletions covering the N-terminal regions of COL4A5 and COL4A6, which are localized in a head-to-head manner, are found in the chromosome Xq22.3 centromeric deletion syndrome. This results in a phenotype with features of diffuse leiomyomatosis and Alport syndrome (DL-ATS). Belongs to the type IV collagen family. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; Extracellular matrix; Secreted; Secreted, signal peptide Chromosomal Location of Human Ortholog: Xq22 Cellular Component: endoplasmic reticulum lumen; extracellular region Biological Process: collagen catabolic process; extracellular matrix organization and biogenesis Disease: Alport Syndrome, X-linked |
| UniProt Code: | P29400 |
| NCBI GenInfo Identifier: | 461675 |
| NCBI Gene ID: | 1287 |
| NCBI Accession: | P29400.2 |
| UniProt Secondary Accession: | P29400,Q16006, Q16126, Q6LD84, Q7Z700, Q9NUB7, |
| Molecular Weight: | 161,632 Da |
| NCBI Full Name: | Collagen alpha-5(IV) chain |
| UniProt Protein Name: | Collagen alpha-5(IV) chain |
| Protein Family: | Collagen |
| UniProt Gene Name: | COL4A5 |
| UniProt Entry Name: | CO4A5_HUMAN |
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