COL4a5 antibody (AA 1462-1691)
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- Target See all COL4a5 (COL4A5) Antibodies
- COL4a5 (COL4A5) (Collagen, Type IV, alpha 5 (COL4A5))
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Binding Specificity
- AA 1462-1691
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This COL4a5 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- SSVAHGFLIT RHSQTTDAPQ CPQGTLQVYE GFSLLYVQGN KRAHGQDLGT AGSCLRRFST MPFMFCNINN VCNFASRNDY SYWLSTPEPM PMSMQPLKGQ SIQPFISRCA VCEAPAVVIA VHSQTIQIPH CPQGWDSLWI GYSFMMHTSA GAEGSGQALA SPGSCLEEFR SAPFIECHGR GTCNYYANSY SFWLATVDVS DMFSKPQSET LKAGDLRTRI SRCQVCMKRT
- Cross-Reactivity
- Human
- Characteristics
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1462-1691 of human COL4A5 (NP_203699.1).
- Isotype
- IgG
- Top Product
- Discover our top product COL4A5 Primary Antibody
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- Application Notes
- WB,1:500 - 1:2000
- Comment
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- COL4a5 (COL4A5) (Collagen, Type IV, alpha 5 (COL4A5))
- Alternative Name
- COL4A5 (COL4A5 Products)
- Background
- 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.,COL4A5,ASLN,ATS,CA54,COL4A5
- Molecular Weight
- 161 kDa
- Gene ID
- 1287
- UniProt
- P29400
- Pathways
- Skeletal Muscle Fiber Development
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