ARG58616

anti-FECH antibody

anti-FECH antibody for ICC/IF,Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes FECH
Tested Reactivity Hu, Ms
Predict Reactivity Cow, Rat, Dog, Gpig, Hrs, Rb, Yeast, Zfsh
Tested Application ICC/IF, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name FECH
Antigen Species Human
Immunogen Synthetic peptide around the N-terminal region of Human FECH. (within the following sequence: LDRDLMTLPIQNKLAPFIAKRRTPKIQEQYRRIGGGSPIKIWTSKQGEGM)
Conjugation Un-conjugated
Alternate Names EPP; EC 4.99.1.1; Ferrochelatase, mitochondrial; FCE; Protoheme ferro-lyase; Heme synthase

Application Instructions

Predict Reactivity Note Predicted homology based on immunogen sequence: Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Rabbit: 100%; Rat: 100%; Yeast: 77%; Zebrafish: 86%
Application Suggestion
Tested Application Dilution
ICC/IFAssay-dependent
WB2.5 µg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Jurkat

Properties

Form Liquid
Purification Purification with Protein A.
Buffer PBS, 0.09% (w/v) Sodium azide and 2% Sucrose.
Preservative 0.09% (w/v) Sodium azide
Stabilizer 2% Sucrose
Concentration Batch dependent: 0.5 - 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 2235 Human FECH

Swiss-port # P22830 Human Ferrochelatase, mitochondrial

Gene Symbol FECH
Gene Full Name ferrochelatase
Background The protein encoded by this gene is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome 3.[provided by RefSeq, May 2010]
Function Catalyzes the ferrous insertion into protoporphyrin IX. [UniProt]
Calculated MW 48 kDa