Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation)

Atlas Antibodies

Catalog No.:
ATL-HPA029198-100
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Protein Description: serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
Gene Name: SERPINH1
Alternative Gene Name: CBP1, CBP2, colligen, HSP47, SERPINH2
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000070436: 89%, ENSRNOG00000016831: 88%
Entrez Gene ID: 871
Uniprot ID: P50454
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

Product Specifications
Application WB, ICC, IHC
Reactivity Human, Mouse
Clonality Polyclonal
Host Rabbit
Immunogen LSAFCLLEAALAAEVKKPAAAAAPGTAEKLSPKAATLAERSAGLAFSLYQAMAKDQAVENILVSPVVVASSLGLVSLGGKATTASQAKAVLSAEQLRDEEVHAGLGELLRSLSNSTARNVTWKL
Gene Sequence LSAFCLLEAALAAEVKKPAAAAAPGTAEKLSPKAATLAERSAGLAFSLYQAMAKDQAVENILVSPVVVASSLGLVSLGGKATTASQAKAVLSAEQLRDEEVHAGLGELLRSLSNSTARNVTWKL
Gene ID - Mouse ENSMUSG00000070436
Gene ID - Rat ENSRNOG00000016831
Buffer 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.

Documents & Links for Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation)
Datasheet Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation) at Atlas Antibodies

Documents & Links for Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation)
Datasheet Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation)
Citations for Anti SERPINH1 pAb (ATL-HPA029198 w/enhanced validation) – 1 Found
Macken, William L; Godwin, Annie; Wheway, Gabrielle; Stals, Karen; Nazlamova, Liliya; Ellard, Sian; Alfares, Ahmed; Aloraini, Taghrid; AlSubaie, Lamia; Alfadhel, Majid; Alajaji, Sulaiman; Wai, Htoo A; Self, Jay; Douglas, Andrew G L; Kao, Alexander P; Guille, Matthew; Baralle, Diana. Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly. Genome Medicine. 2021;13(1):34.  PubMed